Dr Ram Manohar Lohia Hospital Tender

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Dr Ram Manohar Lohia Hospital Tender

Goods
Healthcare and Medicine
Eprocure
Opening Date21 Dec 2023
Closing Date20 Jan 2024
Tender AmountRefer Documents 
Notes
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Costs

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OXYGENATOR MEMBRANE (PAED.)WITH HARD SHELL RESERVOIR STERILE. (2) 1. Should have a microporus hollow fiber membrane Oxygenator. 2. Should have open circuit configuration. 3. Should have hard shell venous reservoir of capacity more than 1000ml. With built of cardiotomy reservoir with 30µ filter capacity. 4. Should have blood flow upto 2.8 ltr/min. 5. Should have priming volume less than 140ml 6. Should have high efficiency heat exchanger. 7. Venous return port 3/8” with rotating facility and reducers. 8. Should have an auto vent facility. 9. Port size : arterial outlet 1/4”, Venous inlet 3/8” with reducers.

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OXYGENATOR MEMBRANE (NEONATAL) STERILE.OXYGENATOR MEMBRANE (NEONATAL) STERILE.(3) Should have venous inlet %". Arterial outlet port 1/4" tubing size. It should have least priming volume less than 70m1. Arterial flow upto 1.2 ltr/minute Approximate Reservoir capacity should be 600m1. Should have reducers. Blood inlet and outlet port size %" reduce able to 3/16". Should have FDA/ EuroPean CE (from notified body) /BIS approved.

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PRE.CONNECTED TUBING PACK ADULT WITH ARTERIAL LINE FILTER STERILE. 1. Circuit Diagram attached.(4) 2. Tubing should have transparent ,medical implant grade PVC of class VI USP, European CE (from notified body) marked 3. Should have FDA/ European CE (from notified body) /BIS approved

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PRE-CONNECTED TUBING PACK PAED. WTftI ARTERIAL LINE FILTER STERILE. (5)(A) 1. Circuit Diagram attached 2. Tubing should have transparent ,medical implant grade PVC of class VI USP, European CE (from notified body) marked 3. Should have FDA/ European CE (from notified body) /BIS approved.

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PRE-CONNECTED TUBING PACK PAEDIATRIC SMALL. WITH ARTERIAL LINE FILTER STERILE. (5)(B) l Circuit Diagram attached 2. Tubing should have transparent ,medical implant grade PVC of class VI USP, European CE (from notified body) marked 3. Should have FDA/ European CE (from notified body) /BIS approved.

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PRE-CONNECTED TUBING PACK NEONATAL. WITH ARTERIAL LINE FILTER STERILE. (6) 1. Circuit Diagram attached. 2. It should have a good quality arterial filter pore size should have 35-40 Micron. 3. Tubing should have transparent medical implant grade PVC of class VI USP, European CE (from notified body) marked. 4. Should have FDA/ European CE (from notified body) /BIS approved.1. Circuit Diagram attached.

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ONLINE BLOOD CARDIOPLEGIA DELIVERY SYSTEM STERILE.(7) 1. Should have in built high efficiency heat exchanger of metallic for fast cooling & re-warming. 2. Should have priming volume less than 80m1. 3. Should have max flow rate 1 Itr/min 4. Should have pressure drop not more than 13mmhg 500m1/min 5. Should have blood to crystalloid ratio of 4:1 with bride connection facilities and interchangeable tubing ratio. 6. Should have auto-vent line system on accidental bock of cardioplegia deliver liner. 7. PVC Tubing should have medical implant grade of class VI ,USP, European CE (from notified bodY) marked. 8. Should have FDA/ EuroPean CE (from notified bodY) /BIS approved.

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ANTE. GRADE ROOT CARDIOPLEGIA CANNULA.STERILE. (8)(A)(I) 1. Should have Size 12G. 2. Should have regular tip stilate with side arm for vent with flange 3. Selection strictly on quality basis. 4. Should have FDA/ EuroPean CE (from notified body) /BIS approved.

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ANTE- GRADE ROOT CARDIOPLEGIA CANNULA. STERILE.(II) 1. Should have Size 14 G. 2. Should have regular tip stilate with side arm for vent with flange 3. Selection strictly on quality basis. 4. Should have FDA/ European CE (from notified body) /BIS approved.be 600m1.

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ANTE- GRADE ROOT CARDIOPLEGIA CANNULA. STERILE. (III) 1. Should have Size 16 G. 2. Should have regular tip stilate with side arm for vent with flange 3. Selection strictly on quality basis. 4, Should have FDA/ European CE (from notified body) /BIS approved.

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ANTE- GRADE ROOT CARDIOPLEGI-A CANNULA WITHOUT SIDE ARM STERILE. (B)(I) 1. Should have Size 12G. 2. Should have regular tip stllate with flange 3. Selection strictly on quality basis. 4. FDA/ European CE (from notlfied body) /ISO Certification

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ANTE- GRADE ROOT CARDIOPLEGI-A CANNULA WITHOUT SIDE ARM STERILE.(II) 1. Should have Size 14 G 2. Should have regular tip stilate with flange 3. Selection strictly on quality basis. 4. FDA/ European CE (from notified body)/ISO Certification

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ANTE. GRADE ROOT CARDIOPLEGI-A CANNULA WITHOUT SIDE ARM STERILE.(III) 1. Should have Size 16 G. 2. Should have regular tip stilate with flange 3. Selection strictly on quality basis. 4. FDA/ European CE (from notified body) /ISO Certification

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CORONARY OSNAL CANNULA STERILE. (9)(A)(I) 1. Should have malleable shaft, female luer lock, radio opaque flower tip selection strictly on quallty basis. 2. Size 14 Fr 3. Should have FDA/ European CE (from notified body) /BIS approved.

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CORONARY OSNAL CANNULA STERILE. (II) 1. Should have malleable shaft, female luer lock, radio opaque flower tip selectionstrictly on quality basis. 2. Size 12 Fr . 3. Should have FDA/ European CE (from notified body) /BIS approved.

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CORONARY OSNAL CANNULA STERILE. (III) 1. Should have malleable shaft, female luer lock, radio opaque flower tip selection strictly on quality basis. 2. Size 10 Fr. 3. Should have FDA/ European CE (from notified body) /BIS approved.

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CORONARY OSNAL CANNULA STERILE. (B)(I) 1. Should have flexible silicon PVC tubing, female luer lock, radio opaque ball tip selection strictly on quality basis. 2. Size l2Fr 3. Should have FDA/ European CE (from notified body) /BIS approved

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CORONARY OSNAL CANNULA STERILE. (II) 1. Should have flexible silicon /PVC tubing, female luer lock, radio opaque ball tip selection strictly on quality basis. 2. Size 10 Fr 3. Should have FDA/ European CE (from notified body) /BIS approved.

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CORONARY OSNAL CANNULA STERILE. (III) 1. Should have flexible silicon/ PVC tubing, female luer lock, radio opaque ball tip selection strictly on quality basis. 2. Size 14 Fr 3. Should have FDA/ European CE (from notified body) /BIS approved

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RETROGRADE CARDIOPLEGIA CANNULA STERILE. (10) 1. It should auto inflatable balloon. 2. It should have pressure measuring line with 3 way connector. 3. It should with malleable stylet / built stylet . 4. Should have FDA/ European CE (from notified body) /BIS approved.

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VENT CATHETER (ADULT) STERILE. (11)(A)(I) 1. Should have flexible with malleable stilate and multiple side hole at the tip of cannula 2. Should have FDA/ European CE (from notified body) /BIS approved. 3. Size : l7Fr.

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VENT CATHETER (ADULT) STERILE. (II) 1. Should have flexible with malleable stylet / built s{let and multiple side hole at the tip of cannula 2. Should have FDA/ European CE (from notified body) /BIS approved. 3. Size : 18 Fr.

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VENT CATHETER (ADULT) STERILE.(III) 1. Should have flexible with malleable stylet / in built stylet and multiple side hole at the tip of cannula 2. Should have FDA/ European CE (from notified body) /BIS approved. 3. Size : 19 Fr.

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VENT CATHETER (ADULT) STERILE.(IV) 1. Should have flexible with malleable stylet /In built stylet in and multiple side hole at the tip of cannula 2. Should have FDA/ European CE (from notified body) /BIS approved. 3. Size: 20 Fr.

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VENT CATHETER (ADULT) STERILE.(V) 4. Should have flexible with malleable stylet/ built stylet and multiple side hole at the tip of cannula 5. Should have FDA/ European CE (from notified body) /BIS approved. 6. Size : 16 Fr.

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VENT CATHETER (ADULT) . STERILE WITH ONE WAY VALVE (B)(I) 1. Should have flexible with malleable stylet / built stylet and multiple side hole at the tip of cannula 2. Should have one way valve to preventair embolization. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size : 14 Fr

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VENT CATHETER (ADULT) . STERILE WITH ONE WAY VALVE (II) 1. Should have flexible with malleable stylet / built stylet and multiple side hole at the tip of cannula 2. Should have one way valve to preventair embolization. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size :15Fr.

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VENT CATHETER (ADULT) . STERILE WITH ONE WAY VALVE (III) 1.Should have flexible with malleable stylet / built stylet and multiple side hole at the tip of cannula 2.Should have one way valve to preventair embolization. 3 Should have FDA/ European CE (from notified body)/BIS approved. 4. Size : 16 Fr.

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VENT CATHETER (ADULT) . STERILE WITH ONE WAY VALVE (IV) 1.Should have flexible with malleable stylet / built stylet and multiple side hole at the tip of cannula 2.Should have one way valve to preventair embolization. 3 Should have FDA/ European CE (from notified body)/BIS approved. 4. Size : 17 Fr.

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VENT CATHETER (ADULT) . STERILE WITH ONE WAY VALVE (V) 1.Should have flexible with malleable stylet / built stylet and multiple side hole at the tip of cannula 2.Should have one way valve to preventair embolization. 3 Should have FDA/ European CE (from notified body)/BIS approved. 4. Size : 18 Fr.

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VENT CATHETER (ADULT) . STERILE WITH ONE WAY VALVE (VI) 1.Should have flexible with malleable stylet / built stylet and multiple side hole at the tip of cannula 2.Should have one way valve to preventair embolization. 3 Should have FDA/ European CE (from notified body)/BIS approved. 4. Size : 19 Fr.

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VENT CATHETER (ADULT) . STERILE WITH ONE WAY VALVE (VII) 1.Should have flexible with malleable stylet / built stylet and multiple side hole at the tip of cannula 2.Should have one way valve to preventair embolization. 3 Should have FDA/ European CE (from notified body)/BIS approved. 4. Size : 20 Fr.

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VENT CATHETER (PEAD.) STERILE.(12)(I) 1. Should have flexible with malleable stylet / built stylet and multiPle side hole at the tip of cannula 2. Size - 10 fr. 3. Should have FDA/ European CE (from notified body) /BIS approved.

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VENT CATHETER (PEAD.) STERILE. (I) 1. Should have flexible with malleable stylet / built stylet and multiPle side hole at the tip of cannula 2. Size - 12 fr. 3. Should have FDA/ European CE (from notified body) /BIS approved.

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VENT CATHETER (PEAD.) STERILE. (III) 1. Should have flexible with malleable stylet / built stylet and multiPle side hole at the tip of cannula 2. Size - 13 fr. 3. Should have FDA/ European CE (from notified body) /BIS approved.

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VENT CATHETER (PEAD.) STERILE.(IV) 1. Should have flexible with malleable stylet / built stylet and multiple side hole at the tip of cannula 2. Size – 14 fr. 3. Should have FDA/ European CE (from notified body) /BIS approved.

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VENT CATHETER (PEAD.) (V) 1. Should have flexible with malleable stylet / built stylet and multiple side hole at the tip of cannula 2. Size – 15 fr. 3. Should have FDA/ European CE (from notified body) /BIS approved.

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RIGHT ANGLE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE. (13)(I) 1. Should have flexible wire reinforce with plastic/metallic angled tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size : 10 Fr.

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RIGHT ANGLE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE. (I) 1. Should have flexible wire reinforce with plastic/metallic angled tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size : 12 Fr.

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RIGHT ANGLE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(III) 1. Should have flexible wire reinforce with plastic/metallic angled tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size : 14 Fr.

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RIGHT ANGLE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE. (IV) 1. Should have flexible wire reinforce with plastic/metallic angled tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size : 16 Fr.

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RIGHT ANGLE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(V) 1. Should have flexible wire reinforce with plastic/metallic angled tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size : 18 Fr.

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RIGHT ANGLE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(VI) 1. Should have flexible wire reinforce with plastic/metallic angled tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size : 20 Fr.

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RIGHT ANGLE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(VII) 1. Should have flexible wire reinforce with plastic/metallic angled tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size : 22 Fr.

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RIGHT ANGLE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(VIII) 5. Should have flexible wire reinforce with plastic/metallic angled tip. 6. Should have depth marking assist with positing. 7. Should have FDA/ European CE (from notified body) /BIS approved. 8. Size : 24 Fr.

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RIGHT ANGLE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(IX) 9. Should have flexible wire reinforce with plastic/metallic angled tip. 10. Should have depth marking assist with positing. 11. Should have FDA/ European CE (from notified body) /BIS approved. 12. Size : 26Fr.

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RIGHT ANGLE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(X) 1. Should have flexible wire reinforce with plastic/metallic angled tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size : 28 Fr.

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RIGHT ANGLE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(XI) 1. Should have flexible wire reinforce with plastic/metallic angled tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size : 30 Fr.

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SINGLE STAGE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(14) (I) 1. Should have flexible wire reinforce, multiple side hole with smooth tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size : 10 Fr

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SINGLE STAGE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE. (II) 1. Should have flexible wire reinforce, multiple side hole with smooth tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size : 12 Fr

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SINGLE STAGE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(III) 1. Should have flexible wire reinforce, multiple side hole with smooth tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size : 14 Fr

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SINGLE STAGE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(IV) 1. Should have flexible wire reinforce, multiple side hole with smooth tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size : 16 Fr

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SINGLE STAGE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(V) 1. Should have flexible wire reinforce, multiple side hole with smooth tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size : 18 Fr

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SINGLE STAGE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(VI) 1. Should have flexible wire reinforce, multiple side hole with smooth tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size : 20 Fr

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SINGLE STAGE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(VII) 1. Should have flexible wire reinforce, multiple side hole with smooth tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size : 22 Fr

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SINGLE STAGE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(VIIII) 1. Should have flexible wire reinforce, multiple side hole with smooth tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size : 24 Fr

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SINGLE STAGE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(IX) 1. Should have flexible wire reinforce, multiple side hole with smooth tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from 1500notified body) /BIS approved. 4. Size : 26 Fr

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SINGLE STAGE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(X) 1. Should have flexible wire reinforce, multiple side hole with smooth tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size : 28 Fr

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SINGLE STAGE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(XI) 1. Should have flexible wire reinforce, multiple side hole with smooth tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size : 30 Fr

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SINGLE STAGE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(XII) 1. Should have flexible wire reinforce, multiple side hole with smooth tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size :32 Fr

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SINGLE STAGE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(XIII) 1. Should have flexible wire reinforce, multiple side hole with smooth tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size : 34 Fr

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SINGLE STAGE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(XIV) 1. Should have flexible wire reinforce, multiple side hole with smooth tip. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size : 36 Fr

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TWO STAGE SINGLE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.15 (I) 1. Should have flexible wire reinforce, multiple side hole with smooth tip with side hole and stilate. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size 32 x 40 Fr

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TWO STAGE SINGLE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(II) 1. Should have flexible wire reinforce, multiple side hole with smooth tip with side hole and stilate. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size 34 x 46 Fr

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TWO STAGE SINGLE VENOUS CANNULA WITH WIRE RE-IN-FORCED STERILE.(III) 1. Should have flexible wire reinforce, multiple side hole with smooth tip with side hole and stilate. 2. Should have depth marking assist with positing. 3. Should have FDA/ European CE (from notified body) /BIS approved. 4. Size 36 x 46,Fr

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TWO STAGE SINGLE VENOUS CANNULA FLAT WITH WIRE RE-IN-FORCED STERILE.16(I) 1. Should have flexible wire reinforce, multiple side hole with smooth tip with side hole and stilate. 2. Should have flat in middle 3. Should have depth marking assist with positing. 4. Should have FDA/ European CE (from notified body) /BIS approved. 5. Size 32 x 40 Fr

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TWO STAGE SINGLE VENOUS CANNULA FLAT WITH WIRE RE-IN-FORCED STERILE(II) 1. Should have flexible wire reinforce, multiple side hole with smooth tip with side hole and stilate. 2. Should have flat in middle 3. Should have depth marking assist with positing. 4. Should have FDA/ European CE (from notified body) /BIS approved. 5. Size 34 x 46Fr

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TWO STAGE SINGLE VENOUS CANNULA FLAT WITH WIRE RE-IN-FORCED STERILE.(III) 1. Should have flexible wire reinforce, multiple side hole with smooth tip with side hole and stilate. 2. Should have flat in middle 3. Should have depth marking assist with positing. 4. Should have FDA/ European CE (from notified body) /BIS approved. 5. Size 36 x 46Fr.

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MIST BLOWER STERILE.17 1. Should have malleable tip with air filter . 2. Should have uniform mixing gas and fluid. 3. Should have flower shape of spray. Should have separate gas and iv fluid port. 4. FDA/ European CE (from notified body) /ISO Certification

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INTRA CORONARY SHUNT 18 A (I) 1. Should be flexible, sterile and smooth side bulb in both end. 1. Should have thread with button 2. Size 1mm 3. Should have FDA/ European CE (from notified body) /BIS approved.

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INTRA CORONARY SHUNT SEMI FLEXIBLE WITH WIRE-REINFORCED (II) Should be semi flexible, sterile and smooth side bulb in both end and shunt should be wire-reinforced. Should have thread with button Size 1mm Should have FDA/ European CE (from notified body) /BIS approved.

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INTRA CORONARY SHUNT (III) 1. Should be flexible ,sterile and smooth side bulb in both end. 2. Should have thread with button 3. Size 1.25mm 4. Should have FDA/ European CE (from notified body) /BIS approved.

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INTRA CORONARY SHUNT SEMI FLEXIBLE WITH WIRE-REINFORCED (IV) Should be semi flexible, sterile and smooth side bulb in both end and shunt should be wire-reinforced. Should have thread with button Size 1.25mm Should have FDA/ European CE (from notified body) /BIS approved.

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INTRA CORONARY SHUNT (V) 1. Should be flexible,sterile and smooth side bulb in both end 2. Should have thread with button 3. Size 1.5mm 4. Should have FDA/ European CE (from notified body) /BIS approved.

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INTRA CORONARY SHUNT SEMI FLEXIBLE WITH WIRE-REINFORCED(VI) Should be semi flexible, sterile and smooth side bulb in both end and shunt should be wire-reinforced. Should have thread with button Size 1.5mm Should have FDA/ European CE (from notified body) /BIS approved.

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INTRA CORONARY SHUNT (VII) 1. Should be flexible,sterile and smooth side bulb in both end. 2. Should have thread with button 3. Size 1.75mm 4. Should have FDA/ European CE (from notified body) /BIS approved.

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INTRA CORONARY SHUNT SEMI FLEXIBLE WITH WIRE-REINFORCED(VIII) Should be semi flexible, sterile and smooth side bulb in both end and shunt should be wire-reinforced. Should have thread with button Size 1.75mm Should have FDA/ European CE (from notified body) /BIS approved.

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INTRA CORONARY SHUNT (IX) 1. Should be flexible,sterile and smooth side bulb in both end. 2. Should have thread with button. 3. Size 2.0mm 4. Should have FDA/ European CE (from notified body) /BIS approved.

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INTRA CORONARY SHUNT SEMI FLEXIBLE WITH WIRE-REINFORCED (X) Should be semi flexible, sterile and smooth side bulb in both end and shunt should be wire-reinforced. Should have thread with button Size 2.0mm Should have FDA/ European CE (from notified body) /BIS approved.

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INTRA CORONARY SHUNT (XI) 1. Should be flexible,sterile and smooth side bulb in both end. 2. Should have thread with button 3. Size 2.25mm 4. Should have FDA/ European CE (from notified body) /BIS approved.

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INTRA CORONARY SHUNT SEMI FLEXIBLE WITH WIRE-REINFORCED(XII) Should be semi flexible, sterile and smooth side bulb in both end and shunt should be wire-reinforced. Should have thread with button Size 2.25mm Should have FDA/ European CE (from notified body) /BIS approved.

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INTRA CORONARY SHUNT (XIII) 1. Should be flexible,sterile and smooth side bulb in both end. 2. Should have thread with button 3. Size 2.5mm 4. Should have FDA/ European CE (from notified body) /BIS approved.

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INTRA CORONARY SHUNT 1. Should be flexible,sterile and smooth side bulb in both end. 2. Should have thread with button 3. Size 2.5mm 4. Should have FDA/ European CE (from notified body) /BIS approved.

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INTRA CAROTID SHUNTS STERILE.(B) 1.Should be Flexible 2. 2. It should have inflatable balloon in both ends of the lumen (shunts) 3. 3 Should have FDA/ European CE (from notified body) /BIS approved.

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CORONARY ARTERY RETRECTION CLIP. (C)(I) 1. It should have malleable wire for better exposure. 2. Size- 3mm 3. Should have FDA/ European CE (from notified body) /BIS approved.

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CORONARY ARTERY RETRECTION CLIP.(II) 1. It should have malleable wire for better exposure. 2. Size- 4mm 3. Should have FDA/ European CE (from notified body) /BIS approved.

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CORONARY ARTERY RETRECTION CLIP.(III) 4. It should have malleable wire for better exposure. 5. Size- 5mm. 6. Should have FDA/ European CE (from notified body) /BIS approved.

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CONNECTORS STRAIGHT STERILE. (19)(A)(I) 1. It should be sterile and transparent 2. Size Required: ½ x ½” 3. Should have FDA/ European CE (from notified body) /BIS approved.

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CONNECTORS STRAIGHT STERILE.(II) 1. It should be sterile and transparent 2. Size Required: ½ x 3/8” 3. Should have FDA/ European CE (from notified body) /BIS approved.

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CONNECTORS STRAIGHT STERILE.(III) 1. It should be sterile and transparent 2. Size Required: 3/8 x 3/8” 3. Should have FDA/ European CE (from notified body) /BIS approved.

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CONNECTORS STRAIGHT STERILE.(IV) 1. It should be sterile and transparent 2. Size Required: 3/8 x ¼” 3. Should have FDA/ European CE (from notified body) /BIS approved.

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CONNECTORS STRAIGHT STERILE.(V) 1. It should be sterile and transparent 2. Size Required: ¼ x ¼” 3. Should have FDA/ European CE (from notified body) /BIS approved.

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CONNECTORS STRAIGHT STERILE. (VI) 1. It should be sterile and transparent 2. Size Required: ¼ x 3/16 3. Should have FDA/ European CE (from notified body) /BIS approved.

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CONNECTORS STRAIGHT STERILE.(VII) 1. It should be sterile and transparent 2. Size Required: 3/16 x 3/16 3. Should have FDA/ European CE (from notified body) /BIS approved.

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CONNECTOR WITH LUER LOCK STERILE.(B)(I) 1. It should be sterile and transparent 2. Sizes - ½ x ½”

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CONNECTOR WITH LUER LOCK STERILE.(II) 1. It should be sterile and transparent 2. Sizes - 3/8 x 3/8”

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CONNECTOR WITH LUER LOCK STERILE.(III) 1) It should be sterile and transparent 2) Sizes - 1/4 x 1/4,

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CONNECTOR WITH LUER LOCK STERILE.(IV) 1. It should be sterile and transparent 2. Sizes - 3/8 x 3/8

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CONNECTOR WITH LUER LOCK STERILE. (V) 1) It should be sterile and transparent 2) Sizes - ¼ x ¼ x ¼

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CONNECTOR WITH LUER LOCK STERILE.(VI) 1) It should be sterile and transparent 2) Sizes - ¼ x 3/16

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CONNECTOR WITH LUER LOCK STERILE.(VII) 1) It should be sterile and transparent 2) Sizes - 3/16 x 3/16

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Y- CONNECTORS STERILE.(20)(A)(I) 1. It should be sterile and transparent 2. Size : ½ x 3/8 x 3/8 3. Should have FDA/ European CE (from notified body) /BIS approved.

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Y- CONNECTORS STERILE.(II) 1. It should be sterile and transparent 2. Size : 3/8 x 3/8 x 3/8 3. Should have FDA/ European CE (from notified body) /BIS approved.

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Y- CONNECTORS STERILE.(III) 1. It should be sterile and transparent 2. Size : 3/8 x3/8 x ¼ 3. Should have FDA/ European CE (from notified body) /BIS approved.

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Y- CONNECTORS STERILE.(IV) 1. It should be sterile and transparent 2. Size : ¼ x ¼ x 3/8 3. Should have FDA/ European CE (from notified body) /BIS approved.

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Y-CONNECTORS STERILE.(B) 1. It should be sterile and transparent 2. Size : ¼ x ¼ x ¼ 3. Should have FDA/ European CE (from notified body) /BIS approved.

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FEMORAL VENOUS (PERFUSION) CANNULA STERILE.(21)(A)(I) 1. Should have flexible with wire-re-in forced built in connector with dilator. 2. Should have FDA/ European CE (from notified body) Certification. 3. Size--10 Fr

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FEMORAL VENOUS (PERFUSION) CANNULA STERILE.(II) 1. Should have flexible with wire-re-in forced built in connector with dilator. 2. Should have FDA/ European CE (from notified body) Certification. 3. Size--12 Fr

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FEMORAL VENOUS (PERFUSION) CANNULA STERILE.(III) 1. Should have flexible with wire-re-in forced built in connector with dilator. 2. Should have FDA/ European CE (from notified body) Certification. 3. Size—14 Fr

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FEMORAL VENOUS (PERFUSION) CANNULA STERILE.(IV) 1. Should have flexible with wire-re-in forced built in connector with dilator. 2. Should have FDA/ European CE (from notified body) Certification. 3. Size--15 Fr

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FEMORAL VENOUS (PERFUSION) CANNULA STERILE.(V) 1. Should have flexible with wire-re-in forced built in connector with dilator. 2. Should have FDA/ European CE (from notified body) Certification. 3. Size--16 Fr

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FEMORAL VENOUS (PERFUSION) CANNULA STERILE.(VI) 1. Should have flexible with wire-re-in forced built in connector with dilator. 2. Should have FDA/ European CE (from notified body) Certification. 3. Size--17 Fr

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FEMORAL VENOUS (PERFUSION) CANNULA STERILE.(VII) 1. Should have flexible with wire-re-in forced built in connector with dilator. 2. Should have FDA/ European CE (from notified body) Certification. 3. Size--18 Fr

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FEMORAL VENOUS (PERFUSION) CANNULA STERILE.(VIII) 1. Should have flexible with wire-re-in forced built in connector with dilator. 2. Should have FDA/ European CE (from notified body) Certification. 3. Size--19 Fr

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FEMORAL VENOUS (PERFUSION) CANNULA STERILE.(IX) 1. Should have flexible with wire-re-in forced built in connector with dilator. 2. Should have FDA/ European CE (from notified body) Certification. 3. Size--20 Fr

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FEMORAL VENOUS (PERFUSION) CANNULA STERILE.(X) 1. Should have flexible with wire-re-in forced built in connector with dilator. 2. Should have FDA/ European CE (from notified body) Certification. 3. Size--21 Fr

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FEMORAL VENOUS (PERFUSION) CANNULA STERILE.(XI) 1. Should have flexible with wire-re-in forced built in connector with dilator. 2. Should have FDA/ European CE (from notified body) Certification. 3. Size--22 Fr

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FEMORAL VENOUS (PERFUSION) CANNULA STERILE.(XII) 1. Should have flexible with wire-re-in forced built in connector with dilator. 2. Should have FDA/ European CE (from notified body) Certification. 3. Size--23 Fr

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FEMORAL VENOUS (PERFUSION) CANNULA STERILE.(XIII) 1. Should have flexible with wire-re-in forced built in connector with dilator. 2. Should have FDA/ European CE (from notified body) Certification. 3. Size--24 Fr

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MULTISTAGE FEMORAL VENOUS (PERFUSION) CANNULA STERILE.(B)(I) 1. Should have flexible with wire-re-in forced built in connector with dilator. 2. It should have multistage for better venous drainage. 3. Should have FDA/ European CE (from notified body) Certification 4. All sizes. 5. Should have FDA/ European CE (from notified body) /BIS approved. 6 Size-- 17

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MULTISTAGE FEMORAL VENOUS (PERFUSION) CANNULA STERILE(II) 1. Should have flexible with wire-re-in forced built in connector with dilator. 2. It should have multistage for better venous drainage. 3. Should have FDA/ European CE (from notified body) Certification 4. All sizes. 5. Should have FDA/ European CE (from notified body) /BIS approved. 6. Size-- 18

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MULTISTAGE FEMORAL VENOUS (PERFUSION) CANNULA STERILE.(III) 1. Should have flexible with wire-re-in forced built in connector with dilator. 2. It should have multistage for better venous drainage. 3. Should have FDA/ European CE (from notified body) Certification 4. All sizes. 5. Should have FDA/ European CE (from notified body) /BIS approved. 6. Size-- 19

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MULTISTAGE FEMORAL VENOUS (PERFUSION) CANNULA STERILE.(IV) 1) Should have flexible with wire-re-in forced built in connector with dilator. 2) It should have multistage for better venous drainage. 3) Should have FDA/ European CE (from notified body) Certification 4) All sizes. 5) Should have FDA/ European CE (from notified body) /BIS approved. 6) Size-- 20

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MULTISTAGE FEMORAL VENOUS (PERFUSION) CANNULA STERILE.(V) 1. Should have flexible with wire-re-in forced built in connector with dilator. 2. It should have multistage for better venous drainage. 3. Should have FDA/ European CE (from notified body) Certification 4. All sizes. 5. Should have FDA/ European CE (from notified body) /BIS approved. 6. Size-- 21

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MULTISTAGE FEMORAL VENOUS (PERFUSION) CANNULA STERILE.(VI) 7. Should have flexible with wire-re-in forced built in connector with dilator. 8. It should have multistage for better venous drainage. 9. Should have FDA/ European CE (from notified body) Certification 10. All sizes. 11. Should have FDA/ European CE (from notified body) /BIS approved. 12. Size-- 22

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MULTISTAGE FEMORAL VENOUS (PERFUSION) CANNULA STERILE.(VII) 13. Should have flexible with wire-re-in forced built in connector with dilator. 14. It should have multistage for better venous drainage. 15. Should have FDA/ European CE (from notified body) Certification 16. All sizes. 17. Should have FDA/ European CE (from notified body) /BIS approved. 18. Size-- 23

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FEMORAL ARTERIO- VENOUS (PERFUSION) CANNULA KIT FOR PERCUTANEOUS INSERTION STERILE.(22) Femoreal Arterial -Venous cannula one each with dilator and insertion kit for minimal invasive cardiac surgery. Kit should have two seldinger stylet needles. Four dilators to guide wire length more than 140cm scalpel blade. Should have FDA/ European CE (from notified body) /BIS approved.

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FEMORAL - ARTERIAL (PERFUSION) CANNULA STERILE.(23)(I) Should have flexible with wire-re-in forced built in connector with dilators Size- -10fr Should have FDA/ European CE (from notified body) /BIS approved.

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FEMORAL - ARTERIAL (PERFUSION) CANNULA STERILE.(II) Should have flexible with wire-re-in forced built in connector with dilators Size- -12fr Should have FDA/ European CE (from notified body) /BIS approved.

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FEMORAL - ARTERIAL (PERFUSION) CANNULA STERILE.(III) Should have flexible with wire-re-in forced built in connector with dilators Size- -14fr Should have FDA/ European CE (from notified body) /BIS approved.

1

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FEMORAL - ARTERIAL (PERFUSION) CANNULA STERILE.(IV) Should have flexible with wire-re-in forced built in connector with dilators Size- -15fr Should have FDA/ European CE (from notified body) /BIS approved.

1

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FEMORAL - ARTERIAL (PERFUSION) CANNULA STERILE.(V) Should have flexible with wire-re-in forced built in connector with dilators Size- -16fr Should have FDA/ European CE (from notified body) /BIS approved.

1

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FEMORAL - ARTERIAL (PERFUSION) CANNULA STERILE.(VI) Should have flexible with wire-re-in forced built in connector with dilators Size- -17fr Should have FDA/ European CE (from notified body) /BIS approved.

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FEMORAL - ARTERIAL (PERFUSION) CANNULA STERILE.(VII) Should have flexible with wire-re-in forced built in connector with dilators Size- -18fr Should have FDA/ European CE (from notified body) /BIS approved.

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FEMORAL - ARTERIAL (PERFUSION) CANNULA STERILE.(VIII) Should have flexible with wire-re-in forced built in connector with dilators Size- -19fr Should have FDA/ European CE (from notified body) /BIS approved.

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FEMORAL - ARTERIAL (PERFUSION) CANNULA STERILE.(IX) Should have flexible with wire-re-in forced built in connector with dilators Size- -20fr Should have FDA/ European CE (from notified body) /BIS approved.

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FEMORAL - ARTERIAL (PERFUSION) CANNULA STERILE.(X) Should have flexible with wire-re-in forced built in connector with dilators Size- -21fr Should have FDA/ European CE (from notified body) /BIS approved.

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FEMORAL - ARTERIAL (PERFUSION) CANNULA STERILE.(XI) Should have flexible with wire-re-in forced built in connector with dilators Size- -22fr Should have FDA/ European CE (from notified body) /BIS approved.

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FEMORALARTERIAL (PERFUSION) CANNULA STERILE.(XII) Should have flexible with wire-re-in forced built in connector with dilators Size- -23fr Should have FDA/ European CE (from notified body) /BIS approved.

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TIE BAND STERILE.(24) Should have FDA/ European CE (from notified body) /BIS approved.

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AORTIC CANNULA WITH CURVE TIP STERILE.(25)(A) A (1) (i) Should have wire reinforced, side flange with Curved tip Size: 16 Fr Should have FDA/ European CE (from notified body) /BIS approved.

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Should have wire reinforced, side flange with (A)(1)(II) Curved tip Size: 18 Fr Should have FDA/ European CE (from notified body) /BIS approved.

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Should have wire reinforced, side flange with (A)(1)(III) Curved tip Size: 20 Fr Should have FDA/ European CE (from notified body) /BIS approved.

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Should have wire reinforced, side flange with (A)(1)(IV) Curved tip Size: 22 Fr Should have FDA/ European CE (from notified body) /BIS approved.

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Should have wire reinforced, side flange with (A)(1)(V) Curved tip Size: 24 Fr Should have FDA/ European CE (from notified body) /BIS approved.

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Should have transparent, side flange with (A)(2)(I) Curved tip Size: 16 Fr Should have FDA/ European CE (from notified body) /BIS approved.

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Should have transparent, side flange with (A)(2)(II) Curved tip Size: 18 Fr Should have FDA/ European CE (from notified body) /BIS approved.

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Should have transparent, side flange with (A)(2)(III) Curved tip Size: 20 Fr Should have FDA/ European CE (from notified body) /BIS approved.

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Should have transparent, side flange with (A)(2)(IV) Curved tip Size: 22 Fr Should have FDA/ European CE (from notified body) /BIS approved.

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Should have transparent, side flange with (A)(2)(V) Curved tip Size: 24 Fr Should have FDA/ European CE (from notified body) /BIS approved.

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AORTIC CANNULA WITH STRAIGHT TIP STERILE.(B) 1. Should have straight tip with side flange for fixation with auto venting facilities 2. Should have FDA/ European CE (from notified body) /BIS approved.

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PAEDIATRIC AORTIC CANNULA. STERILE.(26)(I) 1. Should have wire reinforced built in connector straight tip with movable auto venting stilate for easy cannulation 2. Size : 8 Fr 3. Should have FDA/ European CE (from notified body) /BIS approved.

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PAEDIATRIC AORTIC CANNULA. STERILE.(II) 1. Should have wire reinforced built in connector straight tip with movable auto venting stilate for easy cannulation 2. Size : 9 Fr 3. Should have FDA/ European CE (from notified body) /BIS approved.

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PAEDIATRIC AORTIC CANNULA. STERILE.(III) 1. Should have wire reinforced built in connector straight tip with movable auto venting stilate for easy cannulation 2. Size : 10 Fr 3. Should have FDA/ European CE (from notified body) /BIS approved.

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PAEDIATRIC AORTIC CANNULA. STERILE.(IV) 1. Should have wire reinforced built in connector straight tip with movable auto venting stilate for easy cannulation 2. Size : 11Fr 3. Should have FDA/ European CE (from notified body) /BIS approved.

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PAEDIATRIC AORTIC CANNULA. STERILE.(V) 1. Should have wire reinforced built in connector straight tip with movable auto venting stilate for easy cannulation 2. Size : 12 Fr 3. Should have FDA/ European CE (from notified body) /BIS approved.

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PAEDIATRIC AORTIC CANNULA. STERILE.(VI) 1. Should have wire reinforced built in connector straight tip with movable auto venting stilate for easy cannulation 2. Size : 13Fr 3. Should have FDA/ European CE (from notified body) /BIS approved.

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PAEDIATRIC AORTIC CANNULA. STERILE.(VII) 1. Should have wire reinforced built in connector straight tip with movable auto venting stilate for easy cannulation 2. Size : 14 Fr 3. Should have FDA/ European CE (from notified body) /BIS approved.

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PAEDIATRIC AORTIC CANNULA. STERILE.(VIII) 1. Should have wire reinforced built in connector straight tip with movable auto venting stilate for easy cannulation 2. Size : 15 Fr 3. Should have FDA/ European CE (from notified body) /BIS approved.

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PAEDIATRIC AORTIC CANNULA. STERILE.(IX) 1. Should have wire reinforced built in connector straight tip with movable auto venting stilate for easy cannulation 2. Size : 16 Fr 3. Should have FDA/ European CE (from notified body) /BIS approved.

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ARTERIAL FILTER PAEDIATRICSTERILE.(27) Priming volume should not more than 70ml filter size should be 35 to 40µ Attached 3/8” Dia. Tubing Loop Should have FDA/ European CE (from notified body) /BIS approved.

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STERILE PACKING TUBING PVC STERILE.(28)(I) Size : ½” Dia. Of 10 feet length tubing. Tubing should have medical implant grade of class VI PVC, USP, European CE (from notified body) marked. Should have FDA/ European CE (from notified body) /BIS approved.

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STERILE PACKING TUBING PVC STERILE.(II) Size : 3/8” Dia. Of 10 feet length tubing. Tubing should have medical implant grade of class VI PVC, USP, European CE (from notified body) marked. Should have FDA/ European CE (from notified body) /BIS approved.

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STERILE PACKING TUBING PVC STERILE.(III) Size : ¼” Dia. Of 10feet length tubing. Tubing should have medical implant grade of class VI PVC, USP, European CE (from notified body) marked. Should have FDA/ European CE (from notified body) /BIS approved.

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CARDIOPLEGIA CANNULA PAED. STERILE.(29) A.) Should be with stilate and side flange for fixation. Size 18 g length of approx. 6.5cm Should have FDA/ European CE (from notified body) /BIS approved.

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B.) Should be with stilate and side flange for fixation. Size 18 g length of approx. 16cm Should have FDA/ European CE (from notified body) /BIS approved.

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CONONARY OSTIAL CANNULAOF SILICON OR PVC WITH SIDE BULB(30)(A)(I) Size-Paed Should have FDA/ European CE (from notified body) /BIS approved

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CONONARY OSTIAL CANNULAOF SILICON OR PVC WITH SIDE BULB(II) Size-Neonatal Should have FDA/ European CE (from notified body) /BIS approved.

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ARTRIOTOMY CANNULA STERILE.(B)(I) Should have a polyurethane tube with bulb with female luer lock Sizes 2mm tip Should have FDA/ European CE (from notified body) /BIS approved.

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ARTRIOTOMY CANNULA STERILE.(II) Should have a polyurethane tube with bulb with female luer lock Sizes 4mm tip Should have FDA/ European CE (from notified body) /BIS approved.

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ARTRIOTOMY CANNULA STERILE.(III) Should have a polyurethane tube with bulb with female luer lock Sizes 6mm tip Should have FDA/ European CE (from notified body) /BIS approved.

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IMA CANNULA WITH BALL TIP STERILE.(31) Should have FDA/ European CE (from notified body) /BIS approved.

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DOUBLE LUMAN VENOUS (PERFUSION CANNULA) STERILE.(32)(I) For veno- venous ECMO Support. Should have blood inlet and outlet port with connector Should have FDA/ European CE (from notified body) /BIS approved. Size Pediatric

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DOUBLE LUMAN VENOUS (PERFUSION CANNULA) STERILE.(II) For veno- venous ECMO Support. Should have blood inlet and outlet port with connector Should have FDA/ European CE (from notified body) /BIS approved. Size Adult

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HAEMCONCENTRATOR ADULT STERILE.(33)(A) a. It should have high efficiency hemoconcentrator with material of polysulphone / polypropylene b. It should have membrane surface area of 1.0m2 or variable to ± 0.1 M2. c. Primary volume of should be less than 90ml d. Transmembrane pressure should have not more than 500 mmhg. e. It should be with tubing attached/separate for in and out port & Bag. Should have FDA/ European CE (from notified body) /BIS approved.

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HAEMCONCENTRATOR PEADIATRIC STERILE(B) a. It should have high efficiency hemoconcentrator with material of polysulphone / polypropylene. b. It should have membrane surface area of 0.7 m2 or variable to ± 0.1 M2 c. Primary volume of should be less than 70ml. d. Tran membrane pressure should not be more than 500 mmhg. f. It should be with tubing attached/separate for in, out port & Bag Should have FDA/ European CE (from notified body) /BIS approved.

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HAEMCONCENTRATOR NEONATAL STERILE.(C) a. It should have high efficiency hemoconcentrator with material of polysulphone / polypropylene. b. It should have membrane surface area of 0.2 m2 or variable to ± 0.1 M2 c. Primary volume should not be more than 30ml d. Transmembrane pressure should not be more than 500 mmhg. g. It should be with tubing attached/separate for in and out port & Bag. h. Should have FDA/ European CE (from notified body) /BIS approved.

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ADULT CARDIAC SUCKER STERILE.(34)(A) It should be plastic bullet tip with handle compatible in ¼”tubing. Tip size-5cm ± 0.5cm Should have FDA/ European CE (from notified body) /BIS approved.

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PAEDIATRIC CARDIAC SUCKER STERILE.(B) It should small in size, plastic bullet tip with handle compatible in ¼”tubing Tip size-2.5cm ± 0.5cm Should have FDA/ European CE (from notified body) /BIS approved.

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PERICARDIAL/ INTRACARDIAL SUMPS STERILE.(C)(I) Should have fluted tip Encased stainless steel sprig. Tip is attached to soft flexible tubing ending with connector. Sizes 12 Fr Should have FDA/ European CE (from notified body) /BIS approved.

1

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PERICARDIAL/ INTRACARDIAL SUMPS STERILE.(II) Should have fluted tip Encased stainless steel sprig. Tip is attached to soft flexible tubing ending with connector. Sizes 14fr Should have FDA/ European CE (from notified body) /BIS approved.

1

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PERICARDIAL/ INTRACARDIAL SUMPS STERILE.(III) Should have fluted tip Encased stainless steel sprig. Tip is attached to soft flexible tubing ending with connector. Sizes 16fr. Should have FDA/ European CE (from notified body) /BIS approved.

1

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DISPOSABLE PRESSURE TRANSDUCER KIT. STERILE.(35)(A)(I) Kit should be with disposable transducer set with all accessory should be compatible with the present set of monitors. Should have integrated flushing device. Should have different color coding for arterial ,cvp and pa. require in single transducer kit pack Should have FDA/ European CE (from notified body) /BIS approved.

1

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DISPOSABLE PRESSURE TRANSDUCER KIT. STERILE.(II) Kit should be with disposable transducer set with all accessory should be compatible with the present set of monitors. Should have integrated flushing device. Should have different color coding for arterial ,cvp and pa. require in double transducer kit pack. Should have FDA/ European CE (from notified body) /BIS approved.

1

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PRESSURE TRANSDUCER KIT FOR CLOSE BLOOD SAMPLING.STERILE.(B)(I) Kit should be with disposable transducer set with all accessory and cable. should be compatible with the present set of monitors. Should have auto flushing device with reservoir . It should have self ceiling port for close blood sampling to prevent blood loss and infection. Size - Adult Should have FDA/ European CE (from notified body) /BIS approved.

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PRESSURE TRANSDUCER KIT FOR CLOSE BLOOD SAMPLING.STERILE.(II) Kit should be with disposable transducer set with all accessory and cable. should be compatible with the present set of monitors. Should have auto flushing device with reservoir . It should have self ceiling port for close blood sampling to prevent blood loss and infection. Size - Pediatric. Should have FDA/ European CE (from notified body) /BIS approved.

1

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LEUKOCYTE REDUCING ARTERIAL BLOOD FILTER FOR EXTRACORPOREAL SERVICE. STERILE.(36) a. Should have the following specification. b. Leukocyte reducing 40micron surface modified polyster media to remove activated neutrophils. c. 220 ml prime volume and flow rate of 6L/min. d. Automatic air venting with dedicated air vent e. European CE (from notified body) marked with 3/8 inch barbed inlet and outlet ports and with bypass loop. f. Should have FDA/ European CE (from notified body) /BIS approved.

1

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AORTIC PROXIMAL DEVICE.STERILE.(37) For clampless proximal anastomosis in CABG Surgery for connecting vein graft to Aorta. Should have FDA/ European CE (from notified body) /BIS approved.

1

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BI -LEAFLET TOTALLY SUPRA ANNULAR PROSTHETIC HEART VALVE STERILE.(38) 1. Should be Rotatable ,Pyrolytic Carbon Leaflets with Tungsten for better radiopacity 2. Theb prosthesis shopuld be able to reduce risk of PPM's in small Aortic and calcified Roots with 100% orifice to Annulus Match resulting ratio of 1 3. Should be able to optimize hemodynamics in small a 6. Should have pyrolite Housing with Titanium stiffening band. 7. Should have an opening angle of more then 75 Degree. 8. Should have suture markers on sewing ring for be 9. all common sizes should be available pf valve. Should have FDA/ European CE (from notified body) /BIS approved

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ARTERIAL LINE FILTER FOR PAEDIATRIC USE STERILE.(39) a. Should have the following specification. b. 40micron lock woven polyster screen. c. Prime volume less then 20ml with flow upto 1.2L/min . d. Port design to allow ¼ inch. Tubing. e. Should have FDA/ European CE (from notified body) /BIS approved

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LEUKOCYTE REMOVAL FILTER FOR RED BLOOD TRANSFUSION STERILE(40) 1. Should have the following specification. 2. High efficiency leucocyte removal filter, polyster media, for one unit of whole blood or packed cell. 3. Filter hold up volume of 20ml after recovery and leucocyte residual averaging less than 2x 105/unit. 4. Primes directly with red cells and with self levelling drip chamber. 5. Should have FDA/ European CE (from notified body) /BIS approved

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MICROAGGREGATE FILTER (B.T. FILTER) STERILE.(41) a. Should have the following specification. b. 40micron filter to remove microaggregate, debris and clots from stored or salvaged blood. c. Hold up volume of 20ml. d. Gravity prime. e. Should have FDA/ European CE (from notified body) /BIS approved

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DISPOSABLE CENTRIFUGAL PUMP.ADULT AND PAEDIATRIC.STERILE.(42)(A) Compatible with SARNS centrifugal pump Should have FDA/ European CE (from notified body) /BIS approved.

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DISPOSABLE CENTRIFUGAL PUMP. ADULT AND PAEDIATRIC STERILE.(B)(I) Compatible with Medtronic centrifugal pump adult. Should have FDA/ European CE (from notified body) /BIS approved.

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DISPOSABLE CENTRIFUGAL PUMP.ADULT AND PAEDIATRIC STERILE.(II) Compatible with Medtronic centrifugal pump paediatric. Should have FDA/ European CE (from notified body) /BIS approved.

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DISPOSABLE FLOW CONNECTOR/SENSOR FOR CENTRIFUGAL PUMP (C) (I) Compatible to Medtronic flow probe. Should have FDA/ European CE (from notified body) /BIS approved. Size- 3/8”

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DISPOSABLE FLOW CONNECTOR/SENSOR FOR CENTRIFUGAL PUMP(II) Compatible to Medtronic flow probe. Should have FDA/ European CE (from notified body) /BIS approved. Size- ¼”

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AORTIC PUNCH STERILE.(43)(I) It should have Sharp, dual cutting edge for clean, precise removal It should have a conical tip for easy insertion by straight or button Punch available with tapered cutting blade to increase visibility of cutting site. Size -3 mm Should have FDA/ European CE (from notified body) /BIS approved.

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AORTIC PUNCH STERILE.(II) It should have Sharp, dual cutting edge for clean, precise removal It should have a conical tip for easy insertion by straight or button Punch available with tapered cutting blade to increase visibility of cutting site. Size -3.5 mm Should have FDA/ European CE (from notified body) /BIS approved.

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AORTIC PUNCH STERILE.(III) It should have Sharp, dual cutting edge for clean, precise removal It should have a conical tip for easy insertion by straight or button Punch available with tapered cutting blade to increase visibility of cutting site. Size -4 mm Should have FDA/ European CE (from notified body) /BIS approved.

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AORTIC PUNCH STERILE.(IV) It should have Sharp, dual cutting edge for clean, precise removal It should have a conical tip for easy insertion by straight or button Punch available with tapered cutting blade to increase visibility of cutting site. Size -4.5 mm Should have FDA/ European CE (from notified body) /BIS approved.

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AORTIC PUNCH STERILE.(V) It should have Sharp, dual cutting edge for clean, precise removal It should have a conical tip for easy insertion by straight or button Punch available with tapered cutting blade to increase visibility of cutting site. Size -5 mm Should have FDA/ European CE (from notified body) /BIS approved.

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CAUTRY PLATE WITH CORD AND CONNECTOR FOR COMPATIBILITY. STERILE.(44)(I) Patented safety ring technology with Cord for Adult as universal size ,disposable grounding plates for Electro Surgical use, with thin conformable, tear resistant, fluid resistant, occlusive, polypropylene backing, coated with thick and soft hydrophilic conductive adhesive gel. Plate design to have handling tabs. Should have FDA/ European CE (from notified body) /BIS approved.

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CAUTRY PLATE WITH CORD AND CONNECTOR FOR COMPATIBILITY. STERILE.(II) Patented safety ring technology with Cord for Paediatric as universal size ,disposable grounding plates for Electro Surgical use, with thin conformable, tear resistant, fluid resistant, occlusive, polypropylene backing, coated with thick and soft hydrophilic conductive adhesive gel. Plate design to have handling tabs. Should have FDA/ European CE (from notified body) /BIS approved.

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NEONATAL TRIPLE LUMEN STERILE.(45)(I) Neonatal Tripple Lumen Radio opaque Polyurathane Tripple Lumen Catheter 20, 23, 23G, dilator 5 Fr, introducer needle 21G kit for injecting or infusing different solution and medications. Centimeter marking from 5 to 12cm guide wire should be Nitinol (kink-resistant J guide wire.) Size- 4.5 Fr- Length-8cm. Should have FDA/ European CE (from notified body) /BIS approved.

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NEONATAL TRIPLE LUMEN STERILE.(II) Neonatal Tripple Lumen Radio opaque Polyurathane Tripple Lumen Catheter 20, 23, 23G, dilator 5 Fr, introducer needle 21G kit for injecting or infusing different solution and medications. Centimeter marking from 5 to 12cm guide wire should be Nitinol (kink-resistant J guide wire.) Size- 4.5 Fr- Length-10cm.. Should have FDA/ European CE (from notified body) /BIS approved.

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FOUR LUMEN CATHETER STERILE.(46)(I) PUR four lumen intravenous catheter trey presentation should contain only 4 lumen catheter 8.5 fr , 16, 20cm length with lumen size 16. 18G introducer , 1graduated J guide wire , 1 dilator 1 secondary fixation wing 3 injection caps and 1 scalpel . Should have FDA/ European CE (from notified body) /BIS approved.

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FOUR LUMEN CATHETER STERILE.(II) PUR four lumen intravenous catheter trey presentation should contain only 4 lumen catheter 8.5 fr , 16, 20cm length with lumen size 14. 18G introducer , 1graduated J guide wire , 1 dilator 1 secondary fixation wing 3 injection caps and 1 scalpel . Should have FDA/ European CE (from notified body) /BIS approved.

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FOUR LUMEN CATHETER STERILE.(III) PUR four lumen intravenous catheter trey presentation should contain only 4 lumen catheter 8.5 fr , 16, 20cm length with lumen size 18. 18G introducer , 1graduated J guide wire , 1 dilator 1 secondary fixation wing 3 injection caps and 1 scalpel . Should have FDA/ European CE (from notified body) /BIS approved.

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FEMORAL ARTERIAL CANNULA (ADULT) STERILE.(47)(I) Femoral Arterial Cannula (Adult) Seldinger technique polyethylene with radio opaque line and anti-kink collar and wing hub for skin fixation. Size- 1. 20G- Length 8cm. One transparent Catheter (polyethylene), one introducer needle, should one straight guide wire with flexible tip. Should have FDA/ European CE (from notified body) /BIS approved.

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FEMORAL ARTERIAL CANNULA (ADULT) STERILE.(II) Femoral Arterial Cannula (Adult) Seldinger technique polyethylene with radio opaque line and anti-kink collar and wing hub for skin fixation. Size- 2. 18G- Length 10cm. One transparent Catheter (polyethylene), one introducer needle, should one straight guide wire with flexible tip. Should have FDA/ European CE (from notified body) /BIS approved.

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FEMORAL ARTERIAL CANNULA (ADULT) STERILE.(III) Femoral Arterial Cannula (Adult) Seldinger technique polyethylene with radio opaque line and anti-kink collar and wing hub for skin fixation. Size -. 16G- Length 15 cm. One polyurethane with 5 to 20 cm marking on Catheter, one introducer needle, J Guide wireadvancer, with BLS technique. Should have FDA/ European CE (from notified body) /BIS approved.

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FEMORAL ARTERIAL CANNULA (ADULT) STERILE.(IV) Femoral Arterial Cannula (Adult) Seldinger technique polyethylene with radio opaque line and anti-kink collar and wing hub for skin fixation. Size -. 16G- Length 20cm. One polyurethane with 5 to 20 cm marking on Catheter, one introducer needle, J Guide wireadvancer, with BLS technique. Should have FDA/ European CE (from notified body) /BIS approved.

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FEMORAL ARTERIAL CANNULA (PAED) STERILE.(48)(I) Femoral Arterial Cannula (Paed) Polyurathane with radio opaque line introduced by Seldinger technique with integral Polyurathane extension tube length 4.5cm with fixation wing. Presented in a peel-pack. One polyurathane catheter, one introducer needle, one straight guide wire with flexible tip, one 50 X 50 cm drape sheet. Size- 22G- Length 4 cm. Should have FDA/ European CE (from notified body) /BIS approved.

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FEMORAL ARTERIAL CANNULA (PAED) STERILE.(II) Femoral Arterial Cannula (Paed) Polyurathane with radio opaque line introduced by Seldinger technique with integral Polyurathane extension tube length 4.5cm with fixation wing. Presented in a peel-pack. One polyurathane catheter, one introducer needle, one straight guide wire with flexible tip, one 50 X 50 cm drape sheet. Size- 22G- Length 6 cm. Should have FDA/ European CE (from notified body) /BIS approved.

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FEMORAL ARTERIAL CANNULA (PAED) STERILE.(III) Femoral Arterial Cannula (Paed) Polyurathane with radio opaque line introduced by Seldinger technique with integral Polyurathane extension tube length 4.5cm with fixation wing. Presented in a peel-pack. One polyurathane catheter, one introducer needle, one straight guide wire with flexible tip, one 50 X 50 cm drape sheet. Size- 22G- Length 8 cm. Should have FDA/ European CE (from notified body) /BIS approved.

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FEMORAL ARTERIAL CANNULA (PAED) STERILE.(IV) Femoral Arterial Cannula (Paed) Polyurathane with radio opaque line introduced by Seldinger technique with integral Polyurathane extension tube length 4.5cm with fixation wing. Presented in a peel-pack. One polyurathane catheter, one introducer needle, one straight guide wire with flexible tip, one 50 X 50 cm drape sheet. Size- 22G- Length 20cm. Should have FDA/ European CE (from notified body) /BIS approved.

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SPIRAL LACTO (POLYETHYLENE) TUBING STERILE.(49)(I) Spirally coiled tubing (Polyethylene) for drug infusion with drug comparable refrences. From notified body. Size- 100cm Should have FDA/ European CE (from notified body) /BIS approved.

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SPIRAL LACTO (POLYETHYLENE) TUBING STERILE.(II) Spirally coiled tubing (Polyethylene) for drug infusion with drug comparable refrences. From notified body. Size- 150cm Should have FDA/ European CE (from notified body) /BIS approved.

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SPIRAL LACTO (POLYETHYLENE) TUBING STERILE.(III) Spirally coiled tubing (Polyethylene) for drug infusion with drug comparable refrences. From notified body. Size- 200cm Should have FDA/ European CE (from notified body) /BIS approved.

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SPIRAL LACTO (POLYETHYLENE) TUBING STERILE.(iv) Spirally coiled tubing (Polyethylene) for drug infusion with drug comparable refrences. From notified body. Size- 300cm Should have FDA/ European CE (from notified body) /BIS approved.

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SPIRAL LACTO (POLYETHYLENE) TUBING STERILE.(v) Spirally coiled tubing (Polyethylene) for drug infusion with drug comparable refrences. From notified body. Size- 400cm Should have FDA/ European CE (from notified body) /BIS approved.

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POLYETHYLENE PRESSURE EXTENSION TUBE (50)(i) Polyethylene high pressure extension tube Size- 11cm. Should have drug comparable refrecces . from notified body. FDA/ European CE (from notified body) /BIS approved.

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POLYETHYLENE PRESSURE EXTENSION TUBE(ii) Polyethylene high pressure extension tube Size- 30cm. Should have drug comparable refrecces . from notified body. FDA/ European CE (from notified body) /BIS approved.

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POLYETHYLENE PRESSURE EXTENSION TUBE(iii) Polyethylene high pressure extension tube Size- 50cm. Should have drug comparable refrecces . from notified body. FDA/ European CE (from notified body) /BIS approved.

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POLYETHYLENE PRESSURE EXTENSION TUBE(iv) Polyethylene high pressure extension tube Size- 100cm. Should have drug comparable refrecces . from notified body. FDA/ European CE (from notified body) /BIS approved.

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POLYETHYLENE PRESSURE EXTENSION TUBE(v) Polyethylene high pressure extension tube Size- 150 cm. Should have drug comparable refrecces . from notified body. FDA/ European CE (from notified body) /BIS approved.

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POLYETHYLENE PRESSURE EXTENSION TUBE (vi) Polyethylene high pressure extension tube Size- 200cm. Should have drug comparable refrecces . from notified body. FDA/ European CE (from notified body) /BIS approved.

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ANTI-MICROBIAL IMPREGNATED TRIPLE LUMEN CATHETER STERILE.(51)(i) Impregnated with Anti-microbial agents with Nitinol kink-resistant J guide wire. Adult Size- 7.5 Fr with a ±10 % size variation- Length 16 cm Should have FDA/ European CE (from notified body) /BIS approved.

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ANTI-MICROBIAL IMPREGNATED TRIPLE LUMEN CATHETER STERILE.(ii) Impregnated with Anti-microbial agents with Nitinol kink-resistant J guide wire. Adult Size- 7.5 Fr with a ±10 % size variation- Length 20cm Should have FDA/ European CE (from notified body) /BIS approved.

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ANTI-MICROBIAL IMPREGNATED TRIPLE LUMEN CATHETER STERILE.(iii) Impregnated with Anti-microbial agents with Nitinol kink-resistant J guide wire. Paed Size- 4.5 Fr with a ±10 % size variation - Length 6 cm. Should have FDA/ European CE (from notified body) /BIS approved.

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ANTI-MICROBIAL IMPREGNATED TRIPLE LUMEN CATHETER STERILE.(IV) Impregnated with Anti-microbial agents with Nitinol kink-resistant J guide wire. Paed Size- 4.5 Fr with a ±10 % size variation - Length 12.5cm. Should have FDA/ European CE (from notified body) /BIS approved.

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PUR IV ACCESS DEVICE STERILE.(52)(I) Polyurathane IV access Device Size- 16G Should have FDA/ European CE (from notified body) /BIS approved.

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PUR IV ACCESS DEVICE STERILE.(II) Polyurathane IV access Device Size- 18G Should have FDA/ European CE (from notified body) /BIS approved.

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PUR IV ACCESS DEVICE STERILE.(III) Polyurathane IV access Device Size- 20G Should have FDA/ European CE (from notified body) /BIS approved.

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PUR IV ACCESS DEVICE STERILE.(IV) Polyurathane IV access Device Size- 22G Should have FDA/ European CE (from notified body) /BIS approved.

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DRESSING (FILM) STERILE.(53) (A)(I) A.-ultraresistant thick drape used in under the retractor, ultra absorbent pad keeps surgical site dry, containing modified cellulose for good hemostatic action, bactericide action with total incision covering. Size : 50x50cm, sizes variable to ± 5cm

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DRESSING (FILM) STERILE.(II) A.-ultraresistant thick drape used in under the retractor, ultra absorbent pad keeps surgical site dry, containing modified cellulose for good hemostatic action, bactericide action with total incision covering. Size : 38.15.10 sizes variable to ± 5cm

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DRESSING (FILM) STERILE.(III) A.-ultraresistant thick drape used in under the retractor, ultra absorbent pad keeps surgical site dry, containing modified cellulose for good hemostatic action, bactericide action with total incision covering. Size : 38.30.15 sizes variable to ± 5cm

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DRESSING (FILM) STERILE (IV) A.-ultraresistant thick drape used in under the retractor, ultra absorbent pad keeps surgical site dry, containing modified cellulose for good hemostatic action, bactericide action with total incision covering. Size : 38.45.45 sizes variable to ± 5cm

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DRESSING (FILM) STERILE. (V) A.-ultraresistant thick drape used in under the retractor, ultra absorbent pad keeps surgical site dry, containing modified cellulose for good hemostatic action, bactericide action with total incision covering. Size : 38.45.60 sizes variable to ± 5cm

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DRESSING (FILM) STERILE.(VI) A.-ultraresistant thick drape used in under the retractor, ultra absorbent pad keeps surgical site dry, containing modified cellulose for good hemostatic action, bactericide action with total incision covering. Size : 3591 sizes variable to ± 5cm

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DRESSING (FILM) STERILE.(VII) A.-ultraresistant thick drape used in under the retractor, ultra absorbent pad keeps surgical site dry, containing modified cellulose for good hemostatic action, bactericide action with total incision covering. Size : 6x7cm sizes variable to ± 5cm

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DRESSING (FILM) STERILE.(53)(B)(I) B. Absorbent clear acrylic dressings - transparent wound dressing consisting of a clear, conformable, absorbent pad with a acrylic polymer pad technology enclosed between an outer low friction, breathable, waterproof, viral & bacterial barrier film . Perforated wound contact layer coated with moist skin adhesive .pad size should be slightly short then the dressing size variable to ± 2cm 1. Dressing size: 6 cm x 5 cm, Should have FDA/ European CE (from notified body) /BIS approved.

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DRESSING (FILM) STERILE.(II) B. Absorbent clear acrylic dressings - transparent wound dressing consisting of a clear, conformable, absorbent pad with a acrylic polymer pad technology enclosed between an outer low friction, breathable, waterproof, viral & bacterial barrier film . Perforated wound contact layer coated with moist skin adhesive .pad size should be slightly short then the dressing size variable to ± 2cm 2. Dressing size: 9cm x 6.5cm, Should have FDA/ European CE (from notified body) /BIS approved.

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DRESSING (FILM) STERILE. (III) B. Absorbent clear acrylic dressings - transparent wound dressing consisting of a clear, conformable, absorbent pad with a acrylic polymer pad technology enclosed between an outer low friction, breathable, waterproof, viral & bacterial barrier film . Perforated wound contact layer coated with moist skin adhesive .pad size should be slightly short then the dressing size variable to ± 2cm 3. Dressing size: 7.5cm x 9.5cm, Should have FDA/ European CE (from notified body) /BIS approved.

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DRESSING (FILM) STERILE (IV) B. Absorbent clear acrylic dressings - transparent wound dressing consisting of a clear, conformable, absorbent pad with a acrylic polymer pad technology enclosed between an outer low friction, breathable, waterproof, viral & bacterial barrier film . Perforated wound contact layer coated with moist skin adhesive .pad size should be slightly short then the dressing size variable to ± 2cm 4. Dressing size: 11 cm x 12.5cm, Should have FDA/ European CE (from notified body) /BIS approved.

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DRESSING (FILM) STERILE.(V) B. Absorbent clear acrylic dressings - transparent wound dressing consisting of a clear, conformable, absorbent pad with a acrylic polymer pad technology enclosed between an outer low friction, breathable, waterproof, viral & bacterial barrier film . Perforated wound contact layer coated with moist skin adhesive .pad size should be slightly short then the dressing size variable to ± 2cm 5. Dressing size: 15cm x 15cm, Should have FDA/ European CE (from notified body) /BIS approved.

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DRESSING (FILM) STERILE. (VI) B. Absorbent clear acrylic dressings - transparent wound dressing consisting of a clear, conformable, absorbent pad with a acrylic polymer pad technology enclosed between an outer low friction, breathable, waterproof, viral & bacterial barrier film . Perforated wound contact layer coated with moist skin adhesive .pad size should be slightly short then the dressing size variable to ± 2cm 6. Dressing size: 14.5cm x 15.5cm, Should have FDA/ European CE (from notified body) /BIS approved.

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DRESSING (FILM) STERILE.(VII) B. Absorbent clear acrylic dressings - transparent wound dressing consisting of a clear, conformable, absorbent pad with a acrylic polymer pad technology enclosed between an outer low friction, breathable, waterproof, viral & bacterial barrier film . Perforated wound contact layer coated with moist skin adhesive .pad size should be slightly short then the dressing size variable to ± 2cm 7. Dressing size 8.5cm x 10.7cm, Should have FDA/ European CE (from notified body) /BIS approved.

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DRESSING (FILM) STERILE. (VIII) B. Absorbent clear acrylic dressings - transparent wound dressing consisting of a clear, conformable, absorbent pad with a acrylic polymer pad technology enclosed between an outer low friction, breathable, waterproof, viral & bacterial barrier film . Perforated wound contact layer coated with moist skin adhesive .pad size should be slightly short then the dressing size variable to ± 2cm 8. Dressing size: 20cm x 10cm, Should have FDA/ European CE (from notified body) /BIS approved.

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DRESSING (FILM) STERILE. (IX) B. Absorbent clear acrylic dressings - transparent wound dressing consisting of a clear, conformable, absorbent pad with a acrylic polymer pad technology enclosed between an outer low friction, breathable, waterproof, viral & bacterial barrier film . Perforated wound contact layer coated with moist skin adhesive .pad size should be slightly short then the dressing size variable to ± 2cm 9. Dressing size: 17cm x 19cm Should have FDA/ European CE (from notified body) /BIS approved.

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SURGICAL BRUSH IODINE POVIDONE AND CHLOROHEXIDINE STERILE. (54) 1. With sponge impregnated 12% Povidone –iodine in a 15ml solution of Teepol, P.E.G. and water supplied with nail cleaner. 2. With sponge impregnated 20% chlorohexidine – iodine in a 15ml solution of ISO PROPYLE-Alcohol and water supplied with nail cleaner. 3. Should have FDA/ European CE (from notified body) /BIS approved.

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POLYURATHANE LONG CANNULA STERILE. (55) (I) Size- 16g Should have FDA/ European CE (from notified body) /BIS approved.

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POLYURATHANE LONG CANNULA STERILE. (II) Size- 18g Should have FDA/ European CE (from notified body) /BIS approved.

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POLYURATHANE LONG CANNULA STERILE.(III) Size- 20g Should have FDA/ European CE (from notified body) /BIS approved.

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POLYURATHANE LONG CANNULA STERILE.(IV) Size- 22g Should have FDA/ European CE (from notified body) /BIS approved.

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POLYURATHANE LONG CANNULA STERILE.(V) Size- 24g Should have FDA/ European CE (from notified body) /BIS approved.

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ANTIUAV EXTENSION LINE STERILE.(56)(I) Anti UAV Extension Line for light sensitive drugs Size- 100cm Should have FDA/ European CE (from notified body) /BIS approved.

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ANTIUAV EXTENSION LINE STERILE.(II) Anti UAV Extension Line for light sensitive drugs Size- 150cm Should have FDA/ European CE (from notified body) /BIS approved.

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ANTIUAV EXTENSION LINE STERILE.(III) Anti UAV Extension Line for light sensitive drugs Size- 200cm Should have FDA/ European CE (from notified body) /BIS approved.

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THERMODILUTION CATHETER 5 LUMEN WITH OR SEPARATE INSERTION KITSTERILE.(57) Catheter Should have five lumen Percutaneous Insertion kit with it or separately and should have all accessory . Should have FDA/ European CE (from notified body) /BIS approved.

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TRIPLE LUMEN CVP KIT PAED. STERILE.(58) Lumen size- 18/20/18 G Material polyurathine, J type preferable nitinol guide wire for anti kink. Needle dilator . 5ml Syringe inside the kit Size-5.5 fr. 8cm Should have FDA/ European CE (from notified body) /BIS approved.

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ETO AND PLASMA STERILIZER PACKING PAPER ROLL STERILE.(59)(I) Should have various sizes of packing paper of plasma. Should have FDA/ European CE (from notified body) /BIS approved.

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ETO AND PLASMA STERILIZER PACKING PAPER ROLL STERILE.(II) Should have various sizes of ETO sterilization goods. Should have FDA/ European CE (from notified body) /BIS approved.

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CHEST DRAINAGE CATHETER: STERILE.(60)(I) 1. Thoracic drainage catheter. 2. Extra soft catheter is gentle to the body tissues & most suitable for thoracic drainage. 3. Distal end is open with super smooth large eyes to maximize the drainage from the chest. 4. Proximal end is fitted with specially designed tapered tongue to provide excellent forceps grip and non- traumatic insertion. 5. Catheters are marked at every 2cm from the last eye to ascertain the depth of placement. 6. Sterile, double packed in peelable pouch pack. 7. Should be European CE (from notified body) /BIS approved Sizes-16fr

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CHEST DRAINAGE CATHETER: STERILE.(II) 1. Thoracic drainage catheter. 2. Extra soft catheter is gentle to the body tissues & most suitable for thoracic drainage. 3. Distal end is open with super smooth large eyes to maximize the drainage from the chest. 4. Proximal end is fitted with specially designed tapered tongue to provide excellent forceps grip and non- traumatic insertion. 5. Catheters are marked at every 2cm from the last eye to ascertain the depth of placement. 6. Sterile, double packed in peelable pouch pack. 7. Should be European CE (from notified body) /BIS approved Sizes-18fr

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CHEST DRAINAGE CATHETER: STERILE.(III) 1. Thoracic drainage catheter. 2. Extra soft catheter is gentle to the body tissues & most suitable for thoracic drainage. 3. Distal end is open with super smooth large eyes to maximize the drainage from the chest. 4. Proximal end is fitted with specially designed tapered tongue to provide excellent forceps grip and non- traumatic insertion. 5. Catheters are marked at every 2cm from the last eye to ascertain the depth of placement. 6. Sterile, double packed in peelable pouch pack. 7. Should be European CE (from notified body) /BIS approved Sizes-20fr

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CHEST DRAINAGE CATHETER: STERILE.(IV) 1. Thoracic drainage catheter. 2. Extra soft catheter is gentle to the body tissues & most suitable for thoracic drainage. 3. Distal end is open with super smooth large eyes to maximize the drainage from the chest. 4. Proximal end is fitted with specially designed tapered tongue to provide excellent forceps grip and non- traumatic insertion. 5. Catheters are marked at every 2cm from the last eye to ascertain the depth of placement. 6. Sterile, double packed in peelable pouch pack. 7. Should be European CE (from notified body) /BIS approved Sizes-22fr

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CHEST DRAINAGE CATHETER: STERILE.(V) 1. Thoracic drainage catheter. 2. Extra soft catheter is gentle to the body tissues & most suitable for thoracic drainage. 3. Distal end is open with super smooth large eyes to maximize the drainage from the chest. 4. Proximal end is fitted with specially designed tapered tongue to provide excellent forceps grip and non- traumatic insertion. 5. Catheters are marked at every 2cm from the last eye to ascertain the depth of placement. 6. Sterile, double packed in peelable pouch pack. 7. Should be European CE (from notified body) /BIS approved Sizes-24fr

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CHEST DRAINAGE CATHETER: STERILE.(VI) 1. Thoracic drainage catheter. 2. Extra soft catheter is gentle to the body tissues & most suitable for thoracic drainage. 3. Distal end is open with super smooth large eyes to maximize the drainage from the chest. 4. Proximal end is fitted with specially designed tapered tongue to provide excellent forceps grip and non- traumatic insertion. 5. Catheters are marked at every 2cm from the last eye to ascertain the depth of placement. 6. Sterile, double packed in peelable pouch pack. 7. Should be European CE (from notified body) /BIS approved Sizes-26fr

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CHEST DRAINAGE CATHETER: STERILE.(VII) 1. Thoracic drainage catheter. 2. Extra soft catheter is gentle to the body tissues & most suitable for thoracic drainage. 3. Distal end is open with super smooth large eyes to maximize the drainage from the chest. 4. Proximal end is fitted with specially designed tapered tongue to provide excellent forceps grip and non- traumatic insertion. 5. Catheters are marked at every 2cm from the last eye to ascertain the depth of placement. 6. Sterile, double packed in peelable pouch pack. 7. Should be European CE (from notified body) /BIS approved Sizes-28fr

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CHEST DRAINAGE CATHETER: STERILE.(VIII) 1. Thoracic drainage catheter. 2. Extra soft catheter is gentle to the body tissues & most suitable for thoracic drainage. 3. Distal end is open with super smooth large eyes to maximize the drainage from the chest. 4. Proximal end is fitted with specially designed tapered tongue to provide excellent forceps grip and non- traumatic insertion. 5. Catheters are marked at every 2cm from the last eye to ascertain the depth of placement. 6. Sterile, double packed in peelable pouch pack. 7. Should be European CE (from notified body) /BIS approved Sizes-30 fr

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CHEST DRAINAGE CATHETER: STERILE (IX) 1. Thoracic drainage catheter. 2. Extra soft catheter is gentle to the body tissues & most suitable for thoracic drainage. 3. Distal end is open with super smooth large eyes to maximize the drainage from the chest. 4. Proximal end is fitted with specially designed tapered tongue to provide excellent forceps grip and non- traumatic insertion. 5. Catheters are marked at every 2cm from the last eye to ascertain the depth of placement. 6. Sterile, double packed in peelable pouch pack. 7. Should be European CE (from notified body) /BIS approved Sizes-32fr

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CHEST DRAINAGE CATHETER: STERILE.(X) 1. Thoracic drainage catheter. 2. Extra soft catheter is gentle to the body tissues & most suitable for thoracic drainage. 3. Distal end is open with super smooth large eyes to maximize the drainage from the chest. 4. Proximal end is fitted with specially designed tapered tongue to provide excellent forceps grip and non- traumatic insertion. 5. Catheters are marked at every 2cm from the last eye to ascertain the depth of placement. 6. Sterile, double packed in peelable pouch pack. 7. Should be European CE (from notified body) /BIS approved Sizes-34fr

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CHEST DRAINAGE CATHETER: STERILE.(XI) 1. Thoracic drainage catheter. 2. Extra soft catheter is gentle to the body tissues & most suitable for thoracic drainage. 3. Distal end is open with super smooth large eyes to maximize the drainage from the chest. 4. Proximal end is fitted with specially designed tapered tongue to provide excellent forceps grip and non- traumatic insertion. 5. Catheters are marked at every 2cm from the last eye to ascertain the depth of placement. 6. Sterile, double packed in peelable pouch pack. 7. Should be European CE (from notified body) /BIS approved Sizes-36fr

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ANGLED CHEST DRAINAGE CATHETER : (ISO/CE) STERILE.(61)(I) 1. Thoracic drainage catheter with Angle. 2. Extra soft catheter is gentle to the body tissues & most suitable for thoracic drainage. 3. Distal end is open with super smooth large eyes to maximize the drainage from the chest. 4. Proximal end is fitted with specially designed tapered tongue to provide excellent forceps grip and non- traumatic insertion. 5. Catheters are marked at every 2cm from the last eye to ascertain the depth of placement. 6. Sterile, double packed in peelable pouch pack. Sizes-16fr 7. Should have FDA/ European CE (from notified body) /BIS approved.

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ANGLED CHEST DRAINAGE CATHETER : (ISO/CE) STERILE. (II) 1. Thoracic drainage catheter with Angle. 2. Extra soft catheter is gentle to the body tissues & most suitable for thoracic drainage. 3. Distal end is open with super smooth large eyes to maximize the drainage from the chest. 4. Proximal end is fitted with specially designed tapered tongue to provide excellent forceps grip and non- traumatic insertion. 5. Catheters are marked at every 2cm from the last eye to ascertain the depth of placement. 6. Sterile, double packed in peelable pouch pack. Sizes-18fr 7. Should have FDA/ European CE (from notified body) /BIS approved.

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ANGLED CHEST DRAINAGE CATHETER : (ISO/CE) STERILE. (III) 1. Thoracic drainage catheter with Angle. 2. Extra soft catheter is gentle to the body tissues & most suitable for thoracic drainage. 3. Distal end is open with super smooth large eyes to maximize the drainage from the chest. 4. Proximal end is fitted with specially designed tapered tongue to provide excellent forceps grip and non- traumatic insertion. 5. Catheters are marked at every 2cm from the last eye to ascertain the depth of placement. 6. Sterile, double packed in peelable pouch pack. Sizes-20fr 7. Should have FDA/ European CE (from notified body) /BIS approved.

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ANGLED CHEST DRAINAGE CATHETER : (ISO/CE) STERILE.(IV) 1. Thoracic drainage catheter with Angle. 2. Extra soft catheter is gentle to the body tissues & most suitable for thoracic drainage. 3. Distal end is open with super smooth large eyes to maximize the drainage from the chest. 4. Proximal end is fitted with specially designed tapered tongue to provide excellent forceps grip and non- traumatic insertion. 5. Catheters are marked at every 2cm from the last eye to ascertain the depth of placement. 6. Sterile, double packed in peelable pouch pack. Sizes-22fr 7. Should have FDA/ European CE (from notified body) /BIS approved.

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ANGLED CHEST DRAINAGE CATHETER : (ISO/CE) STERILE. (V) 1. Thoracic drainage catheter with Angle. 2. Extra soft catheter is gentle to the body tissues & most suitable for thoracic drainage. 3. Distal end is open with super smooth large eyes to maximize the drainage from the chest. 4. Proximal end is fitted with specially designed tapered tongue to provide excellent forceps grip and non- traumatic insertion. 5. Catheters are marked at every 2cm from the last eye to ascertain the depth of placement. 6. Sterile, double packed in peelable pouch pack. Sizes-24 fr 7. Should have FDA/ European CE (from notified body) /BIS approved.

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ANGLED CHEST DRAINAGE CATHETER : (ISO/CE) STERILE.(VI) 1. Thoracic drainage catheter with Angle. 2. Extra soft catheter is gentle to the body tissues & most suitable for thoracic drainage. 3. Distal end is open with super smooth large eyes to maximize the drainage from the chest. 4. Proximal end is fitted with specially designed tapered tongue to provide excellent forceps grip and non- traumatic insertion. 5. Catheters are marked at every 2cm from the last eye to ascertain the depth of placement. 6. Sterile, double packed in peelable pouch pack. Sizes-26fr 7. Should have FDA/ European CE (from notified body) /BIS approved.

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ANGLED CHEST DRAINAGE CATHETER : (ISO/CE) STERILE.(VII) 1. Thoracic drainage catheter with Angle. 2. Extra soft catheter is gentle to the body tissues & most suitable for thoracic drainage. 3. Distal end is open with super smooth large eyes to maximize the drainage from the chest. 4. Proximal end is fitted with specially designed tapered tongue to provide excellent forceps grip and non- traumatic insertion. 5. Catheters are marked at every 2cm from the last eye to ascertain the depth of placement. 6. Sterile, double packed in peelable pouch pack. Sizes-28fr 7. Should have FDA/ European CE (from notified body) /BIS approved.

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ANGLED CHEST DRAINAGE CATHETER : (ISO/CE) STERILE.(VIII) 1. Thoracic drainage catheter with Angle. 2. Extra soft catheter is gentle to the body tissues & most suitable for thoracic drainage. 3. Distal end is open with super smooth large eyes to maximize the drainage from the chest. 4. Proximal end is fitted with specially designed tapered tongue to provide excellent forceps grip and non- traumatic insertion. 5. Catheters are marked at every 2cm from the last eye to ascertain the depth of placement. 6. Sterile, double packed in peelable pouch pack. Sizes-30fr 7. Should have FDA/ European CE (from notified body) /BIS approved.

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ANGLED CHEST DRAINAGE CATHETER : (ISO/CE) STERILE.(IX) 1. Thoracic drainage catheter with Angle. 2. Extra soft catheter is gentle to the body tissues & most suitable for thoracic drainage. 3. Distal end is open with super smooth large eyes to maximize the drainage from the chest. 4. Proximal end is fitted with specially designed tapered tongue to provide excellent forceps grip and non- traumatic insertion. 5. Catheters are marked at every 2cm from the last eye to ascertain the depth of placement. 6. Sterile, double packed in peelable pouch pack Sizes-32fr 7. Should have FDA/ European CE (from notified body) /BIS approved.

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ANGLED CHEST DRAINAGE CATHETER : (ISO/CE) STERILE. (X) 1. Thoracic drainage catheter with Angle. 2. Extra soft catheter is gentle to the body tissues & most suitable for thoracic drainage. 3. Distal end is open with super smooth large eyes to maximize the drainage from the chest. 4. Proximal end is fitted with specially designed tapered tongue to provide excellent forceps grip and non- traumatic insertion. 5. Catheters are marked at every 2cm from the last eye to ascertain the depth of placement. 6. Sterile, double packed in peelable pouch pack. Sizes-34fr 7. Should have FDA/ European CE (from notified body) /BIS approved.

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ANGLED CHEST DRAINAGE CATHETER : (ISO/CE) STERILE.(XI) 1. Thoracic drainage catheter with Angle. 2. Extra soft catheter is gentle to the body tissues & most suitable for thoracic drainage. 3. Distal end is open with super smooth large eyes to maximize the drainage from the chest. 4. Proximal end is fitted with specially designed tapered tongue to provide excellent forceps grip and non- traumatic insertion. 5. Catheters are marked at every 2cm from the last eye to ascertain the depth of placement. 6. Sterile, double packed in peelable pouch pack. Sizes-36fr 7. Should have FDA/ European CE (from notified body) /BIS approved.

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UNDER WATER SEAL BOTTLE (CHEST DRAINAGE BOTTLE). (ISO/CE) STRILE. (62) 1. Double chamber compact unit has 2 ltr capacity making it suitable for all cardiac and thoracic procedures. 2. Easy to read graduation help to determine the drainage volume precisely. 3. Clearly marked initial level ensures the under water seal. 4. Separate suction port is provided for connection with suction unit. 5. Kink resistant large bore tubing facilitates unrestricted flow. 6. Unit is provided with metal hangers and floor stand. 7. Should have FDA/ European CE (from notified body) /BIS approved.

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SNUGGER SET STERILE (63)(I) Should have sterile in size of Adult. Should have 3 pairs of snuggers of different colours with S.S snare. Should have FDA/ European CE (from notified body) /BIS approved.

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SNUGGER SET STERILE. (II) Should have sterile in size of paediatric. Should have 3 pairs of snuggers of different colours with S.S snare. Should have FDA/ European CE (from notified body) /BIS approved.

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EMBOLECTOMY CATHETER STERILE. (64)(I) Size 4 fr Should have Sterile FDA/ European CE (from notified body) /BIS approved.

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EMBOLECTOMY CATHETER STERILE. (II) Size5 fr Should have Sterile FDA/ European CE (from notified body) /BIS approved.

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EMBOLECTOMY CATHETER STERILE. (III) Size 6 fr Should have Sterile FDA/ European CE (from notified body) /BIS approved.

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PERITONEAL DIALYSIS CATHETER STERILE. (65)(I) For peritoneal dialysis Size Adult Should have FDA/ European CE (from notified body) /BIS approved.

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PERITONEAL DIALYSIS CATHETER STERILE.(II) For peritoneal dialysis Size Pead Should have FDA/ European CE (from notified body) /BIS approved.

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PERITONEAL DIALYSIS CATHETER STERILE. (III) For peritoneal dialysis Size Neonatal Should have FDA/ European CE (from notified body) /BIS approved.

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GRAFT EMBOLECTOMY CATHETER STERILE.(66)(I) Size 3 fr Should have FDA/ European CE (from notified body) /BIS approved.

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GRAFT EMBOLECTOMY CATHETER STERILE.(II) Size 4 fr Should have FDA/ European CE (from notified body) /BIS approved.

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GRAFT EMBOLECTOMY CATHETER STERILE.(III) Size 5 fr Should have FDA/ European CE (from notified body) /BIS approved.

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GRAFT EMBOLECTOMY CATHETER STERILE.(IV) Size 6 fr Should have FDA/ European CE (from notified body) /BIS approved.

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GRAFT EMBOLECTOMY CATHETER STERILE.(V) Size 7 fr Should have FDA/ European CE (from notified body) /BIS approved.

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ANTI MICROBIAL INCISE DRAPE STERILE (67)(I) Incise drape comprise of polyester, thin, breathable low memory idophor, impregnated film. Drape should be coated with pressure sensitive Acrylate adhesive. Should have FDA/European CE (from notified body)/BIS approved. Size: 34 x 35 cm

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ANTI MICROBIAL INCISE DRAPE STERILE (II) Incise drape comprise of polyester, thin, breathable low memory idophor, impregnated film. Drape should be coated with pressure sensitive Acrylate adhesive. Should have FDA/European CE (from notified body)/BIS approved. Size: 56 x 45 cm

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ANTIMICROBIAL STERILE. DRAPE FOR MINIMALLY INVASIVE SURGERY (68) Polyester film idophor coated with hypo allergic adhesive incise drape differentiated by a frame delivery system for one person application. Size : 26 X20 cm variable to ± 1 cm. Should have FDA/ European CE (from notified body) /BIS approved.

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DISPOSABLE GOWN. STERILE.(69) Should have sterile, impervious yet breathable high performance fabric. Should have abration resistance for liquid barrier. It should have wet microbial resistance and dry microbial resistance. It should have low linting which helps reduce the risk of wound,contamination and infection. It should be free from harm full AZO dyes banned by GOI for environment protection. It should be non irritant ,non sensitizing non cytotoxic to skin. It should have reglan sleeves. It should have adjustable neckline hook and loop fastener. It should have book fold in position. Should have sterile package with two hand towels. Should have latex free,, ETO sterilized. Should have FDA/ European CE (from notified body) /BIS approved.

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STERILE DISP. DRAPE KIT FOR OPEN HEART SURGERY (70)(A) CABG PACK - Sterile Wrap size : 115cm x 115cm, Back Table cover, Reinforced 152cm x 230cm-1pc, Tape Strips 10cm x 55cm -2pcs, suture bags-2pcs, Back Table Cover, Reinforced 140cm x 190cm- 1pc, Utility Drape with Tape 75cm x 75cm-1pc, Perineal Drape 188cm x 242cm with split 45cm x 95cm & positioning tape &control plus fabric reinforcement- 1pc, CV Split Drape 320cm x 224cm x 295cm with positioning tape& control plus fabric reinforcement -1pc. Bar Drape 193cm x 239cm with positioning tape & tube holders & control plus fabric reinforcement- 1pc. Size variable to ± 2cm. It should have FDA/ European CE (from notified body) Certified

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STERILE DISP. DRAPE KIT FOR OPEN HEART SURGERY (B) VALVE REPLACEMENT DRAPE - Drape with size 264cm x 364cm x 194cm, Size variable to ± 2cm With Pouches control Plus Fabric Reinforcement, Tube Holders With one utility drape sheet It should have FDA/ European CE (from notified body) certification

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STERILE DISP. DRAPE KIT FOR OPEN HEART SURGERY (C) Cardiac Procedure Drape with Adhesive Incise Area on Chest & Legs - One Drape With Armboard Covers 108 inch. X 80 inch. X 126 inch, 12 inch. X 15 inch. Chest Adhesive Incise Area, 22 inch. X 38 inch. Leg Adhesive Incise Area, Heavy Duty Fabric, control plus Fabric Reinforcement, Longitudinal Flaps, Tube Holders. It should have FDA/ European CE (from notified body) BIS Approved

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ACT TUBES (71)(A) Compatible with Actalyte ACT machine Should have FDA/ European CE (from notified body) /BIS approved.

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ACT CARTRIDGE (B) It Should have FDA/ European CE (from notified body) /BIS approved. compatible with Medtronic ACT Machine

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VASCULAR GRAFT EPTEE STERILE (72)(A)(I) Size 3 mm x 10cm Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTEE STERILE (II) Size 3.5 mm x 10cm Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTEE STERILE (III) Size 4 mm x 10cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE STERILE(IV) Size 4.5 mm x 10cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE STERILE (V) Size 5 mm x 10cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE STERILE (VI) Size 6 mm x 10cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE STERILE (VII) Size 8 mm x 10cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE STERILE (VIII) Size 6mm x 30cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE STERILE (IX) Size 7mm x 30cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE STERILE (X) Size 8mm x 30cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE STERILE (XI) Size 6mm x 40cm Should have FDA/ European CE (from notified body) /BIS approved

1

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VASCULAR GRAFT EPTEE STERILE (XII) Size 7mm x 40cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE STERILE (XIII) Size 8mm x 40cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE STERILE (XIV) Size 6mm x 50cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE STERILE (XV) Size 7mm x 50cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE STERILE (XVI) Size 8mm x 50cm Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTEE STERILE (XVII) Size 6mm x 60cm Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTEE STERILE (XVIII) Size 7mm x 60cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE STERILE (XIX) Size 8mm x 60cm Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTEE STERILE (XX) Size 6mm x 70cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE STERILE (XXI) Size 7mm x 70cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE STERILE (XXII) Size 8mm x 70cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE STERILE (XXIII) Size 6mm x 80cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE STERILE (XXIV) Size 7mm x 80cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE STERILE (XXV) Size 8mm x 80cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE STERILE (XXVI) Size 6mm x 90cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE STERILE (XXVII) Size 7mm x 90cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE STERILE (XXVIII) Size 8mm x 90cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (72)(B)(I) Size 3 mm x 10cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (II) Size 3.5mm x 10cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (III) Size 4mm x 10cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (IV) Size 4.5 mm x 10cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (V) Size 5 mm x 10cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (VI) Size 6 mm x 10cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (VII) Size 8 mm x 10cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (VIII) Size 6mm x 30cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (IX) Size 7mm x 30cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (X)

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (XI) Size 6mm x 40cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (XII) Size 7mm x 40cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE.(XIII) Size 8mm x 40cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE.(XIV) Size 6mm x 50cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (XV) Size 7mm x 50cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (XVI) Size 8mm x 50cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (XVII) Size 6mm x 60cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (XVIII) Size 7mm x 60cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (XIX) Size 8mm x 60cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (XX) Size 6mm x 70cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (XXI) Size 7mm x 70cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (XXII) Size 8mm x 70cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (XXIII) Size 6mm x 80cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (XXIV) Size 7 mm x 80cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULA GRAFT EPTEE WITH THIN WALL STERILE. (XXV) Size 8mm x 80cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (XXVI) Size 6mm x 90cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (XXVII) Size 7mm x 90cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL STERILE. (XXVIII) Size 8mm x 90cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL AND CARBON COATED STERILE. (73)(C)(I) Size 3 mm x 10cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL AND CARBON COATED STERILE. (II) Size 3.5 mm x 10cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL AND CARBON COATED STERILE. (III) Size 4 mm x 10cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL AND CARBON COATED STERILE. (IV) Size 4.5 mm x 10cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL AND CARBON COATED STERILE. (v) Size 5 mm x 10cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL AND CARBON COATED STERILE. (VI) Size 6mm x 10cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTEE WITH THIN WALL AND CARBON COATED STERILE. (VII) Size 8 mm x 10cm Should have FDA/ European CE (from notified body) /BIS approved.

1

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VASCULAR GRAFT EPTFE STERILE.(74)(D)(I) Size 12 mm X 20 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE. (II) Size 12 mm X 30 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE. (III) Size 12 mm X 40 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE. (IV) Size 14 mm X 20 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE. (V) Size 14 mm X 30 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE. (VI) Size 14 mm X 40 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE. (VII) Size 16 mm X 20 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE. (VIII) Size 16 mm X 30 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE. (IX) Size 16 mm X 40 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE.(x) Size 18 mm X 20 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE.(XI) Size 18 mm X 30 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE. (XII) Size 18 mm X 40 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE. (XIII) Size 19 mm X 20 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE.(XIV) Size 19 mm X 30 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE. (XV) Size 19 mm X 40 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE. (XVI) Size 20 mm X 20 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE.(XVII) Size 20 mm X30 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE. (XVIII) Size 20 mm X 40 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE. (XIX) Size 22 mm X 20 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE.(XX) Size 22 mm X 30 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE.(XXI) Size 22 mm X 40 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE.(XXII) Size 24 mm X 20 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE. (XXIII) Size 24 mm X 30 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT EPTFE STERILE. (XXIV) Size 24 mm X 40 cm length Should have FDA/ European CE (from notified body) /BIS approved.

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SOFT CLOTH REINFORCEMENT DRESSING STERILE. (75)(a)(I) a. Central Venous Catheter dressing with Effective antimicrobial action. Polyurethane Film with Reinforcement of Soft Cloth size 8.5cm x 11.5cm. Single, Sterile, Transparent, Semi-permeable, water and bacteria proof, thin conformable polyurethane film with one half laminated with Soft cloth breathable backing for enhanced grip on challenging and CVC applications. Has a long slit to conform around the CIV and & micro-porous label. Has two extra secural tape for added strength & better securement. With unique paper window frame delivery design

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SOFT CLOTH REINFORCEMENT DRESSING STERILE. (II) a. Central Venous Catheter dressing with Effective antimicrobial action. Polyurethane Film with Reinforcement of Soft Cloth Size: 7 cm x 8.5cm. Single, Sterile, Transparent, Semi-permeable, water and bacteria proof, thin conformable polyurethane film with one half laminated with Soft cloth breathable backing for enhanced grip on challenging and CVC applications. Has a long slit to conform around the CIV and & micro-porous label. Has two extra secural tape for added strength & better securement. With unique paper window frame delivery design

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SOFT CLOTH REINFORCEMENT DRESSING STERILE.(III) a. Central Venous Catheter dressing with Effective antimicrobial action. Polyurethane Film with Reinforcement of Soft Cloth size 6 x 7 cms. Single, Sterile, Transparent, Semi-permeable, water and bacteria proof, thin conformable polyurethane film with one half laminated with Soft cloth breathable backing for enhanced grip on challenging and CVC applications. Has a long slit to conform around the CIV and & micro-porous label. Has two extra secural tape for added strength & better securement. With unique paper window frame delivery design

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SOFT CLOTH REINFORCEMENT DRESSING STERILE. (IV) a. Central Venous Catheter dressing with Effective antimicrobial action. Polyurethane Film with Reinforcement of Soft Cloth size 5 x 5.7 cm. Single, Sterile, Transparent, Semi-permeable, water and bacteria proof, thin conformable polyurethane film with one half laminated with Soft cloth breathable backing for enhanced grip on challenging and CVC applications. Has a long slit to conform around the CIV and & micro-porous label. Has two extra secural tape for added strength & better securement. With unique paper window frame delivery design

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SOFT CLOTH REINFORCEMENT DRESSING STERILE. (b) b. IV Kit with Transparent Dressing for peripheral inserted Catheters : Single Pack Single, Sterile, Transparent, Semi-permeable, water and bacteria proof, thin conformable polyurethane film with one half laminated with Soft cloth breathable backing for enhanced grip on challenging and CVC applications. Has a long slit to conform around the PIV and & micro-porous label. Has two extra secural tape for added strength & better securement. With unique paper window frame delivery design Wipe Impregnated with 2% chlorhexidine Gluconate and 70% isopropyl Achohol, Synthetic polyisoprene based textured surface material of tourniquet (latexfree) Sterile Gauze piece size-7x 6.5cm Should have FDA/ European CE (from notified body) /BIS approved.

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TRANSPARENT DRESSING FOR POST OPP. STERILE. (76)(I) Single sterile Non-adherent absorbent pad (compressed rayon fiber) bonded to a larger soft cloth macro-porous, stretchable, rounded corners backing, coated with a border of hypoallergenic, water-resistant pressure sensitive hypo-allergic adhesive. 6x8cm Size variable to ± 2cm. Should have FDA/ European CE (from notified body) /BIS approved.

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TRANSPARENT DRESSING FOR POST OPP. STERILE. (II) Single sterile Non-adherent absorbent pad (compressed rayon fiber) bonded to a larger soft cloth macro-porous, stretchable, rounded corners backing, coated with a border of hypoallergenic, water-resistant pressure sensitive hypo-allergic adhesive. 9x15cm Size variable to ± 2cm. Should have FDA/ European CE (from notified body) /BIS approved.

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TRANSPARENT DRESSING FOR POST OPP. STERILE.(III) Single sterile Non-adherent absorbent pad (compressed rayon fiber) bonded to a larger soft cloth macro-porous, stretchable, rounded corners backing, coated with a border of hypoallergenic, water-resistant pressure sensitive hypo-allergic adhesive. 9x20cm Size variable to ± 2cm. Should have FDA/ European CE (from notified body) /BIS approved.

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TRANSPARENT DRESSING FOR POST OPP. STERILE. (IV) Single sterile Non-adherent absorbent pad (compressed rayon fiber) bonded to a larger soft cloth macro-porous, stretchable, rounded corners backing, coated with a border of hypoallergenic, water-resistant pressure sensitive hypo-allergic adhesive. 9x25cm Size variable to ± 2cm. Should have FDA/ European CE (from notified body) /BIS approved.

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TRANSPARENT DRESSING FOR POST OPP. STERILE. (V) Single sterile Non-adherent absorbent pad (compressed rayon fiber) bonded to a larger soft cloth macro-porous, stretchable, rounded corners backing, coated with a border of hypoallergenic, water-resistant pressure sensitive hypo-allergic adhesive. 9x30cm Size variable to ± 2cm. Should have FDA/ European CE (from notified body) /BIS approved.

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SOFT CLOTH DRESS. WITH ABS. PAD STERILE (77)(I) Single, Sterile, Transparent, Semi-permeable, water and bacteria proof, thin conformable, polyurethane film coated with water repellant Acrylate hypoallergenic adhesive with paper window frame delivery and having a non adherent absorbent pad (compressed rayon fiber) for very good absorbent and strike through effect. 5x7cm Size variable to ± 2cm. Should have FDA/ European CE (from notified body) /BIS approved.

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SOFT CLOTH DRESS. WITH ABS. PAD STERILE (II) Single, Sterile, Transparent, Semi-permeable, water and bacteria proof, thin conformable, polyurethane film coated with water repellant Acrylate hypoallergenic adhesive with paper window frame delivery and having a non adherent absorbent pad (compressed rayon fiber) for very good absorbent and strike through effect. 8x10cm Size variable to ± 2cm. Should have FDA/ European CE (from notified body) /BIS approved.

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SOFT CLOTH DRESS. WITH ABS. PAD STERILE (III) Single, Sterile, Transparent, Semi-permeable, water and bacteria proof, thin conformable, polyurethane film coated with water repellant Acrylate hypoallergenic adhesive with paper window frame delivery and having a non adherent absorbent pad (compressed rayon fiber) for very good absorbent and strike through effect. 9x15cm Size variable to ± 2cm. Should have FDA/ European CE (from notified body) /BIS approved.

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SOFT CLOTH DRESS. WITH ABS. PAD STERILE (IV) Single, Sterile, Transparent, Semi-permeable, water and bacteria proof, thin conformable, polyurethane film coated with water repellant Acrylate hypoallergenic adhesive with paper window frame delivery and having a non adherent absorbent pad (compressed rayon fiber) for very good absorbent and strike through effect. 9x25cm Size variable to ± 2cm. Should have FDA/ European CE (from notified body) /BIS approved.

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SOFT CLOTH DRESS. WITH ABS. PAD STERILE (V) Single, Sterile, Transparent, Semi-permeable, water and bacteria proof, thin conformable, polyurethane film coated with water repellant Acrylate hypoallergenic adhesive with paper window frame delivery and having a non adherent absorbent pad (compressed rayon fiber) for very good absorbent and strike through effect. 9x35cm Size variable to ± 2cm. Should have FDA/ European CE (from notified body) /BIS approved.

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ON LINE CARDIAC OUTPUT MONITORING TRANSDUCER & KIT STERILE. (78)(A) Compatible with Edward monitor. Should have FDA/ European CE (from notified body) /BIS approved.

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CONTINUOUS CARDIAC OUT PUT MONITIRING SENSOR KIT THROUGHPA STERILE. (B) Continuous cardiac out put monitoring sensor kit for flow directed pulmonary artery catheter enabling monitoring of hemodynamic pressures measurement of mixed venous oxygen saturation and continuous measurement of cardiac output through PA. Should have FDA/ European CE (from notified body) /BIS approved

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EPTFE CARDIOVASCULAR PATCH/MEMBRANE.(79)(I) Thickness – 0.6 mm Sizes 0.6 mm patch (5 x 7.5 cms) Should have FDA/ European CE (from notified body) /BIS approved.

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EPTFE CARDIOVASCULAR PATCH/MEMBRANE. (II) Thickness – 0.4 mm Sizes 0.4 mm patch (3 x 6 cms) Should have FDA/ European CE (from notified body) /BIS approved.

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EPTFE CARDIOVASCULAR PATCH/MEMBRANE. (III) Thickness – 0.1 mm Sizes 0.1 mm thickness patch (6 x 12 cms) Should have FDA/ European CE (from notified body) /BIS approved

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ePTFE FELT SOFT & HARD STERILE. (80)(I) Sizes-5 x 7.5cm Should have FDA/ European CE (from notified body) /BIS approved.

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ePTFE FELT SOFT & HARD STERILE. (II) Sizes-4” x 4” Should have FDA/ European CE (from notified body) /BIS approved.

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DACRON CARDIOVASCULAR PATCH.STERILE. (81)(I) Sizes-4 x 4 inches Should have FDA/ European CE (from notified body) /BIS approved

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DACRON CARDIOVASCULAR PATCH.STERILE. (II) Sizes- 2 x 2 inches Should have FDA/ European CE (from notified body) /BIS approved

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CLOSED CIRCUIT SUCTION SET (82) Should have FDA/ European CE (from notified body) /BIS approved.

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MULTI VESSEL PERFUSION ADAPTOR STERILE. (83) Should have four arm with pinch clamp Should have FDA/ European CE (from notified body) /BIS approved.

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DISPOSABLE TUBING ORGANIZER. STERILE. (84) Should have port for multi sized perfusion tubing e.g. 3/16, ¼, 3/8,1/2,inch tubing. Should have FDA/ European CE (from notified body) /BIS approved

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DOUBLE LUMEN ENDOBRONCHIAL TUBE STERILE. (85)(I) Right Should have with endobronchial blocker Should have FDA/ European CE (from notified body) /BIS approved.

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DOUBLE LUMEN ENDOBRONCHIAL TUBE STERILE. (II) Left Should have with endobronchial blocker Should have FDA/ European CE (from notified body) /BIS approved.

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BIFURCATED RAPID PRIMING SET STERILE (86) Should have 1/4” Bifurcated with “Y” Connector Should have spike in both ends Should have FDA/ European CE (from notified body) /BIS approved.

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EOPA LONG ARTERIAL CANNULA STERILE. (87)(I) Should have sharp tip stylete for easy insertion Should have wire-reinforced. Sizes 16 fr. Should have FDA/ European CE (from notified body) /BIS approved.

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EOPA LONG ARTERIAL CANNULA STERILE. (II) Should have sharp tip stylete for easy insertion Should have wire-reinforced. Sizes 18fr. Should have FDA/ European CE (from notified body) /BIS approved.

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EOPA LONG ARTERIAL CANNULA STERILE. (III) Should have sharp tip stylete for easy insertion Should have wire-reinforced. Sizes 20fr. Should have FDA/ European CE (from notified body) /BIS approved.

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EOPA LONG ARTERIAL CANNULA STERILE. (IV) Should have sharp tip stylete for easy insertion Should have wire-reinforced. Sizes 22fr. Should have FDA/ European CE (from notified body) /BIS approved.

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HME FILTER FOR VENTILATOR CIRCUIT STERILE. (88)(I) Should have sterile For short term humidification. Should have breathing system contamination barrier Should have bacterial, viral filtration efficiencies of 99.9%. Should have FDA/ European CE (from notified body) /BIS approved. Size adult

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HME FILTER FOR VENTILATOR CIRCUIT STERILE. (II) Should have sterile For short term humidification. Should have breathing system contamination barrier Should have bacterial, viral filtration efficiencies of 99.9%. Should have FDA/ European CE (from notified body) /BIS approved. Size pediatric

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LINEAR STAPLER STERILE (89) Should have FDA/ European CE (from notified body) /BIS approved.

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BLADE MANMAN STERNAL SAW (90) Compatible for manman sternal saw Should have FDA/ European CE (from notified body) /BIS approved.

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MONOPOLAR HAND CAUTERY PENCIL (DISPOSABLE) STERILE. (91)(A) 1. It should have universal three pin connector for all kinds of major cautery machines. 2. Should have FDA/ European CE (from notified body) /BIS approved.

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TIP CLEANER (DISPOSABLE) FOR MONOPOLAR HAND CAUTERY PENCIL (B) Tip cleaner should be in the separate sterile packing. Should have FDA/ European CE (from notified body) /BIS approved.

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MONOPOLAR HAND CAUTERY PENCIL (DISPOSABLE) CAUTERY WITH PENCIL TIP CLEANER (DISPOSABLE)STERILE. (C) It should be sterile and supplied in sterile packing with cautery pencil tip cleaner. Should have FDA/ European CE (from notified body) /BIS approved.

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CAUTERY SWITCH WITH POLYURETHAN-E COATED SURGICAL TIP STERILE. (D) Button switch pencil with polytetrafluoroethylene coated electrosurgical tip. Should have FDA/ European CE (from notified body) /BIS approved

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CAUTERY TIP STERILE. (E) Polytetrafluoroethylene coated electrosurgical ball tip, Size – 5 cm Should have FDA/ European CE (from notified body) /BIS approved.

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MALE TO MALE CONNECTOR STERILE. (92) It should have male luer lock in both ends Should have FDA/ European CE (from notified body) /BIS approved.

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VIAL ADAPTER STERILE. (93) For withdrawal of sterile solution from sterile vial to maintain sterility Should have FDA/ European CE (from notified body) /BIS approved.

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EYE SHIELD FOG FREE MASK WITH VISOR (94) 1. It should be consisted fog-free multilayer with visor. 2. It should be made of pleat-style with ties. 3. It should have high fluid resistance capability. 4. It should have particulate filtration efficiency more than 99%. 5. It should have bacterial filtration efficiency more than 99%. 6. Should have FDA/ European CE (from notified body) /BIS approved.

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FLUID SHIELD FOG FREE MASK (95) 1. It should be consisted fog-free multilayer. 2. It should be made of pleat-style with ties. 3. It should have high fluid resistance capability. 4. It should have particulate filtration efficiency more than 99%. 5. It should have bacterial filtration efficiency more than 99%. 6. Should have FDA/ European CE (from notified body) /BIS approved.

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MICROBIAL SEALANT STERILE. (96)(I) 1. It should have antibacterial properties. 2. It should be made of cyanoacrylate technology. 3. It should be capable to seal and immobilizes dangerous pathogens/MRSA. 4. It should be easy-to-use applicator, polymerized in less time. Size: Approximate Coverage: 25cm X 25cm 5. Should have FDA/ European CE (from notified body) /BIS approved.

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MICROBIAL SEALANT STERILE. (II) 1. It should have antibacterial properties. 2. It should be made of cyanoacrylate technology. 3. It should be capable to seal and immobilizes dangerous pathogens/MRSA. 4. It should be easy-to-use applicator, polymerized in less time. Approximate Coverage: 25cm X 50cm 5. Should have FDA/ European CE (from notified body) /BIS approved.

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CARDIOPLEAGIA CANNULA(FOR MINIMAL INVASIVE SURGICAL PROCEDURES) STERILE.(97) 1. It should have a length of more than 30cm with luer connection. 2. It should be supplied with a stainless steel introducer needle. 3. It should be in following sizes 12 ga/9Fr. 4. Should have FDA/ European CE (from notified body) /BIS approved.

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DISPOSABLE SOFT TISSUE RETRACTOR(PROTECTOR) FOR MINIMAL INVASIVE CARDIAC SURGERY STERILE.(98) 1. It should be mode of latex free polymer. 2. It should have high flexibility for easy insert in situ. 3. It should be capable for self holding, for incision from 1 to 14 cm. 4. Should have FDA/ European CE (from notified body) /BIS approved

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DISPOSABLE CORONARY ARTERIOTOMY KNIFE STERILE. (99) 1. It should be sterile with, in built handle. 2. It should have straight sharp pointed tip for Arteriotomy. 3. Tip size should not be more than 1mm. 4. Should be able to make a clear incised Arteriotomy of arteries 1mm in size. 5. Should have FDA/ European CE (from notified body) /BIS approved.

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PAEDIATRIC /NEONATAL TUBING KIT FOR ECMO OXYGENATION STERILE. (100) Tubing should sterile transparent PVC tubing of implant grade vi tubing with flow sensor connector in outlet . 1. It should be pre -reconnected attached with Medtronic compatible centrifugal pump cone . 2. Should have easy for priming without reservoir. 3. PVC tubing size should be 1/4” with complete connector kit and pressure dome . 4. Should have FDA/ European CE (from notified body) /BIS approved.

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ADULT TUBING KIT FOR ECMO OXYGENATION STERILE. (101) 1. Tubing should sterile transparent PVC tubing of implant grade vi tubing with flow sensor connector in outlet . 2. It should be pre -reconnected attached with Medtronic compatible centrifugal pump cone . 3. Should have easy for priming without reservoir. 4. PVC tubing size should be 3/8” with complete connector kit and pressure dome . 5. Should have FDA/ European CE (from notified body) /BIS approved.

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ECMO OXYGENATOR NEONATAL STERILE. (102) 1- It should have long term oxygenation capacity for more than 15 days. 2- It Should have polymethylpentene microporous hollow fiber membrane . 3- It should be sustainable for long term plasma leakage. . 4- It should have integrated heat exchanger. 5- Both Inlet and outlet port size should be 1/4” 6- It should be without centrifugal pump. 7- It should have membrane surface area of 0.6 m2 8- It should be FDA/ European CE (from notified body) approved.

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ECMO OXYGENATOR PAEDIATRIC STERILE. (103) 1- It should have long term oxygenation capacity for more than 15 days . 2- Should have polymethylpentene microporous hollow fiber membrane . 3- It should be sustainable for long term plasma leakage. . 4- It should have integrated heat exchanger . 5- Both Inlet and outlet port size should be 3/8” 6- It should be without centrifugal pump . 7- It should have maximum flow upto or morethan 3 lit/min. 8- It should have membrane surface area of more than 1.2 m 9- Should have FDA/ European CE (from notified body) /BIS approved.

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ECMO OXYGENATOR ADULT STERILE. (104) 1- It should have long term oxygenation capacity for more than 15 days . 2- Should have polymethylpentene microporous hollow fiber membrane . 3- It should be sustainable for long term plasma leakage. . 4- It should have integrated heat exchanger . 5- Both Inlet and outlet port size should be 3/8” 6- It should be without centrifugal pump . 7- It should have maximum flow upto or more than 6 lit/min. 8- It should have membrane surface area of more than 2.4 m2 9- Should have FDA/ European CE (from notified body) /BIS approved.

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DISPOSABLE VASCULAR CLAMP INSERTS STERILE. (105) For better grip and minimizing trauma Should have FDA/ European CE (from notified body) /BIS approved.

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SUTURE ORGANISER DISPOSABLE FOR VALVE SURGERY STERILE. (106) 1. Should be able to stabilize sutures for valve surgery. 2. Should not damage the sutures. 3. Suture should not get entangled. 4. Capable of holding 10-20 sutures 5. Should have FDA/ European CE (from notified body) /BIS approved.

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COMPRESSION ADHESIVE BANDAGE FOR LEG / ARMS STERILE. (107)(I) It should have medical grade bio-compatible, pressure sensitive and trauma free adhesive. It should be breathable latex free. It should have maximum pressure compression for legs or Arms of harvested veins and arteries for coronary grafting. a. 10 cm X 4,5,6 Meter Long. Should have FDA/ European CE (from notified body) /BIS approved.

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COMPRESSION ADHESIVE BANDAGE FOR LEG / ARMS STERILE. (II) It should have medical grade bio-compatible, pressure sensitive and trauma free adhesive. It should be breathable latex free. It should have maximum pressure compression for legs or Arms of harvested veins and arteries for coronary grafting. b. 05 cm X 4,5,6 Meter Long Should have FDA/ European CE (from notified body) /BIS approved.

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SILVER MESH DRESSING STERILE. (108)(I) 1. It should have antimicrobial cotton, Non Woven gauze. 2. It should have soft comfortable impregnated with silver sulphate. 3. It should have various sizes and sizes variable to ± 02 cm 4. Should have FDA/ European CE (from notified body) /BIS approved. 10 cm X 10cm

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SILVER MESH DRESSING STERILE. (II) It should have antimicrobial cotton, Non Woven gauze. It should have soft comfortable impregnated with silver sulphate. It should have various sizes and sizes variable to ± 02 cm. Should have FDA/ European CE (from notified body) /BIS approved. 05 cm X 05 cm

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SILVER MESH DRESSING STERILE. (III) It should have antimicrobial cotton, Non Woven gauze. It should have soft comfortable impregnated with silver sulphate. It should have various sizes and sizes variable to ± 02 cm. Should have FDA/ European CE (from notified body) /BIS approved. 10cmx 20cm

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SILVER MESH DRESSING STERILE. (IV) It should have antimicrobial cotton, Non Woven gauze. It should have soft comfortable impregnated with silver sulphate. It should have various sizes and sizes variable to ± 02 cm. Should have FDA/ European CE (from notified body) /BIS approved. 20cm X 20 cm

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INTRA AORTIC BALLOON CATHETER. STERILE. (109)(I) 1. Should have membrane for improved abrasion resistance. 2. Should have a small profile of7 Fr to 7.5 Fr. 3. Should be available in volume of 30, 34cc, 40cc & 50cc. 4. Balloon diameter at 2psi should be 15mm. 5. Insertable length should not exceed 725mm. 6. Insertion kit should be provided separately. Size 30CC catheter compatible with Data scope IABP Should have FDA/ European CE (from notified body) /BIS approved.

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INTRA AORTIC BALLOON CATHETER. STERILE. (II) 1. Should have membrane for improved abrasion resistance. 2. Should have a small profile of7 Fr to 7.5 Fr. 3. Should be available in volume of 30, 34cc, 40cc & 50cc. 4. Balloon diameter at 2psi should be 15mm. 5. Insertable length should not exceed 725mm. 6. Insertion kit should be provided separately. Size 34 CC catheter compatible with Data scope IABP Should have FDA/ European CE (from notified body) /BIS approved.

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INTRA AORTIC BALLOON CATHETER. STERILE. (III) 1. Should have membrane for improved abrasion resistance. 2. Should have a small profile of7 Fr to 7.5 Fr. 3. Should be available in volume of 30, 34cc, 40cc & 50cc. 4. Balloon diameter at 2psi should be 15mm. 5. Insertable length should not exceed 725mm. 6. Insertion kit should be provided separately. Size 40 CC catheter compatible with Data scope IABP Should have FDA/ European CE (from notified body) /BIS approved.

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INTRA AORTIC BALLOON CATHETER. STERILE. (IV) 1. Should have membrane for improved abrasion resistance. 2. Should have a small profile of7 Fr to 7.5 Fr. 3. Should be available in volume of 30, 34cc, 40cc & 50cc. 4. Balloon diameter at 2psi should be 15mm. 5. Insertable length should not exceed 725mm. 6. Insertion kit should be provided separately. Size 50 CC catheter compatible with Data scope IABP Should have FDA/ European CE (from notified body) /BIS approved.

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ANNULOPLASTY RING, RIGID FOR MITRAL VALVE STERILE. (110) 1. Constructed of titanium alloy with a silicone rubber sewing ring. 2. Closed ring for stable remodelling. 3. Restores the natural size(3:4) & shape in systolic position ratio. 4. Marking sutures for accurate placement. 5. Preferable saddle shaped. Should have FDA/ European CE (from notified body) /BIS approved.

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ANNULOPLASTY RING, MITRAL VALVE FOR ISCHEMIC MR STERILE. (111) Rigid ring for durable repair Complete ring for stable remodelling Asymmetrical design for asymmetrical dilation P2-P3 region Increased sewing ring margin in P2-P3 region. Dipped P3 region to accommodate stress from downward LV displacement Should have FDA/ European CE (from notified body) /BIS approved.

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ANNULOPLASTY RING, SEMI FLEXIBLE/ SEMI RIGID FOR MITRAL VALVE STERILE. (112)(A) Three Dimensional design to Suit the annulus normal of the mitral valve. Semi Flexible in Should have FDA/ European CE (from notified body) /BIS approved.

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ANNULOPLASTY RING, FLEXIBLE FOR MITRAL VALVE STERILE. (B) Barium impregnated silicone strip with polyester fabric for X-Ray visibility. Flexible design to allow dynamic motion Should have FDA/ European CE (from notified body) /BIS approved.

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ANNULOPLASTY RING SEMI RIGID WITH DOUBLE SADDLE SHAPE STERILE (C) 1. For the use of mitral valve repair 2. It should be semi rigid double saddle shaped ring design specially for mitral position for helping stable remodelling. 3. It should have specially crafted sewing cuff has visible ledge that permits placement of sutures. 4. Should have FDA/ European CE (from notified body) /BIS approved.

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ANNULOPLASTY RINGS 3D FOR TRICUSPID VALVE STERILE.(113)(A) Annuloplasty ring with three dimensional shapes with incomplete ring shape to avoid the sensitive conduction system anatomy and downward angle in septal region to help reduce the stress on sutures and the risk of ring dehiscence. Should have FDA/ European CE (from notified body) /BIS approved.

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ANNULOPLASTY RING, SEMI FLEXIBLE FOR TRICUSPID VALVE STERILE. (B) 1. Flexible/ Semi flexible design to allow dynamic annular motion. 2. Open at annuloseptal commissure to avoid conduction system. 3. Should have FDA/ European CE (from notified body) /BIS approved.

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ANNULOPLASTY RING, FLEXIBLE FOR TRICUSPID VALVE STERILE (C) 1. Flexible/ Semi flexible design to allow dynamic annular motion. 2. Open at annuloseptal commissure to avoid conduction system. 3. Should have FDA/ European CE (from notified body) /BIS approved.

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PROSTHETIC HEART VALVE SMALL PROFILE BILEAFLET MITRAL STERILE. (114)(A) 1. Bileaflet pyrolytic carbon disc valve 2. Radioopaque disc to be visualized on x- ray & fluoroscopy and disc should be MRI compatible. 3. Should be of small profile, thromboresistance characteristics, small trnsvalvular gradient and low incidence of mechanical failure. 4. Opening angle should be 750-900 5. Maximum protrusion of leaflet from the housing should not more then 3.5mm. 6. Should have a maximum posterior wall clearance of 6.8mm. 7. Easy torque rotation and intraoperative adjustment should be possible. 8. Sewing cuff should contain suture marker for accurate placement. 9. Valve should have atleast 10 year of clinical data for least valve related complication for patient safety. 10. Should have FDA/ European CE (from notified body).

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PROSTHETIC HEART VALVE BILEAFLET MITRAL STERILE. (B) Bileaflet pyrolytic carbon disc valve. Radioopaque disc to be visualized on x- ray & fluoroscopy and disc should be MRI compatible. Should be of small profile, thromboresistance characteristics, and low incidence of mechanical failure. Opening angle should be 750-900. Easy torque rotation and intraoperative adjustment should be possible. Sewing cuff should contain suture marker for accurate placement. Should have FDA/ European CE (from notified body) /BIS approved.

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PROSTHETIC HEART VALVE SMALL PROFILE BILEAFLET AORTIC VALVE. STERILE. (115)(A) 1. Bi leaflet pyrolytic carbon disc valve 2. Radioopaque disc to be visualized on x- ray & fluoroscopy and disc should be MRI compatible. 3. Should be of small profile & thromboresistance characteristics. 4. Maximum protrusion of leaflet from the housing should not more then 3.5mm. 5. Should have a maximum posterior wall clearance of 6.8mm. 6. Opening angle should be 750-900 7. Easy torque rotation and intraoperative adjustment should be possible. 8. Valve should have atleast 10 year of clinical data for least valve related complication for patient safety 9. Sewing cuff should contain suture marker for accurate placement. 10. Should have FDA/ European CE (from notified body) .

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PROSTHETIC HEART VALVE BILEAFLET AORTIC VALVE. STERILE. (B) Bileaflet pyrolytic carbon disc valve. Radioopaque disc to be visualized on x- ray & fluoroscopy and disc should be MRI compatible. Should be of low profile, thromboresistance characteristics, and low incidence of mechanical failure. Opening angle should be 750-900. Easy torque rotation and intraoperative adjustment should be possible. Sewing cuff should contain suture marker for accurate placement. Should have FDA/ European CE (from notified body) /BIS approved.

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PROSTHETIC HEART VALVE MONO LEAFLET MITRAL & AORTIC STERILE. (116) 1. It should superior hemodynamic. 2. It should be rotatable within the swing ring. 3. It should have rigid tilting disc single leaflet heart valve. 4. Valve should have atleast 10 year of clinical data for least valve related complication for patient safety 5. Should have FDA/ European CE (from notified body approval for imported valve. No FDA/CE approval require for indigenous made heart valve. Should have FDA/ European CE (from notified body) /BIS approved.

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PROSTHETIC HEART VALVE BILEAFLET AORTIC WITH CONDUIT STERILE. STERILE (117) 1. Bileaflet pyrolytic carbon disc valve 2. Radioopaque disc to be visualized on x- ray & fluoroscopy and disc should be MRI compatible. 3. Should be of low profile & thromboresistance characteristics. 4. Maximum protrusion of the leaflet from the housing should not be more then 3.5 mm. 5. Should have a maximum wall clearance 6.8mm. 6. Opening angle should be 750-900 . 7. Wide range of sizes for aortic 8. Easy torque rotation and intra-operative adjustment should be possible. 9. Sewing cuff should contain suture marker for accurate placement. 10. Valve to be European CE (from notified body / FDA approved. 11. Valve should be attached with knitted low porosity coated graft. 12. Valve should have atleast 10 year of clinical data for least valve related complication for patient safety Should have FDA/ European CE (from notified body) /BIS approved.

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LOW PROFILE PROSTHETIC HEART VALVE BILEAFLET AORTIC STERILE. (118) 1. Bileaflet pyrolytic carbon disc valve 2. Radio-opaque disc to be visualized on x- ray & fluoroscopy and disc should be MRI compatible. 3. Should be of low profile & thromboresistance characteristics. 4. Maximum protrusion of the leaflet from the housing should not be more then 3.5mm 5. Should have a maximum posterior wall clearance 6.8 mm. 6. Opening angle should be 750-900 7. Easy torque rotation and intra-operative adjustment should be possible. 8. Sewing cuff should contain suture marker for accurate placement. 9. Valve should have atleast 10 year of clinical data for least valve related complication for patient safety 10. Valve to be European CE (from notified body / FDA approved. Should have FDA/ European CE (from notified body) /BIS approved.

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BIOPROSTHET-IC, HEART VALVE & PERICARDIUMAORTIC & MITRAL STERILE. Specifications. (119)

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STENT – LESS PORCINE TISSUE AORTIC VALVE STERILE. (A) a. Should be made of porcine tissue b. Should be in clinical use with long term good results c. Should have FDA/ European CE (from notified body) /BIS approved.

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STENT-LESS PERICARDIAL TISSUE AORTIC VALVE STERILE (B) a. Should be made of pericardium membrane b. Should be in clinical use with long term good results of more then 15 year. c. Should have FDA/ European CE (from notified body) /BIS approved.

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PERICARDIAL STENTED TISSUE MITRAL VALVE STERILE. (C) a. Should be made of pericardium membrane. b. Second generation valve with anti-calcification treatment. c. Should have long term good results available in literature and more than 15 years durability in vivo. d. Should have FDA/ European CE (from notified body) /BIS approved.

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PERICARDIAL STENTED TISSUE MITRAL VALVE STERILE. (D) a. Low profile third generation valve with anticalcification treatment b. Should have long term good results available in literature and more than 15 years durability in vivo c. Should have FDA/ European CE (from notified body) /BIS approved.

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PERICARDIAL STENTED TISSUE AORTIC VALVE STERILE. (E) a. Second generation with anticalcification treatment b. Should have long term good results available in literature and more than 15 years durability in vivo. Should have FDA/ European CE (from notified body) /BIS approved

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PERICARDIAL STENTED TISSUE MITRAL VALVE STERILE. (F) a. Low profile third generation with anticalcification treatment b. Should have long term good results available in literature and more than 15 years durability in vivo Should have FDA/ European CE (from notified body) /BIS approved.

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PERICARDIAL STENTED TISSUE AORTIC VALVE WITH PERICARDIAL COVERED STENT. STERILE. (G) a. Third generation pericardial stented valve with stunts covered with pericardium and treated with anticalcification technology b. Should have good long term in vitro results available in literature and more than 15 years durability in vivo c. Aortic valve delivered larger eoas, Excellent hemodynamic with single- digit pressure gradients d. Elimination of tacking suture at loupe of commissure reduced risk of tearing e. High strength titanium stunts and quick click in handle attachment f. Should have FDA/ European CE (from notified body) /BIS approved.

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PORCINE BIOPROSTHETIC LOW PROFILE MITRAL AND AORTIC VALVES STERILE. (H) a. Second generation with anti calcification treatment by anticalcification technology b. Low pressure fixation c. Results studied in access of more than 20 years d. Should have FDA/ European CE (from notified body) /BIS approved.

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PORCINE BIOPROSTHETIC LOW PROFILE MITRAL AND AORTIC VALVES STERILE. (I) a. Second generation with anti calcification treatment. b. Low pressure fixation c. Results studied in access of more than 20 years d. Should have FDA/ European CE (from notified body) /BIS approved.

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PORCINE BIOPROSTHETIC LOW PROFILE MITRAL AND AORTIC VALVES STERILE. (J) a. Third generation with anti calcification treatment with covalent bonding with glutraldehyde . b. Physiologic pressure fixation c. Should have FDA/ European CE (from notified body) /BIS approved.

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BOVINE JUGULAR VEIN PULMONARY VALVE CONDUIT (K) Should have FDA/ European CE (from notified body) /BIS approved.

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PULMONARY BIOPROSTHESIS CONDUIT STERILE. (L) Should have FDA/ European CE (from notified body) /BIS approved.

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BOVINE PERICARDIUM STERILE. (M) Pericardium patch Should have FDA/ European CE (from notified body) /BIS approved.

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BIOPROSTHETIC AORTIC VALVE (SUTURE LESS) STERILE. (N) Treated valve to reduce calcification. Should have self expending and elastic alloy stent. Should have covered with film of carbofilm for biocompatibility . Should have FDA/ European CE (from notified body) /BIS approved.

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BOVINE PERICARDIAL STENTED AORTIC DRY STORED TISSUE VALVE STERILE. (O) Aortic bovine pericardial bioprosthetic surgical valve with a three-stage integrity preservation treatment that enables aldehyde-free dry storage, an expandable Co-Cr band and fluoroscopically visible Should have FDA/ European CE (from notified body) /BIS approved.

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BOVINE PERICARDIAL STENTED MITRAL DRY STORED TISSUE VALVE STERILE. (P) Mitral bovine pericardial bioprosthetic surgical valve with a three-stage integrity preservation treatment that enables aldehyde-free dry storage Should have FDA/ European CE (from notified body) /BIS approved.

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HEART STABILIZING SYSTEM STERILE. (120)(A) 1. Tissue stabilizing system with malleable pods for better grip and anastomosis. 2. It should be compatible with various cardiothoracic retractors. 3. It should be suction based. 4. Should be trislot design of pods for better visualization 5. Pods should have low profile design for easy access to any visibility of surgical field with 1800 C rotations. 6. Should have FDA/ European CE (from notified body) /BIS approved.

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HEART STABILIZING SYSTEM (FOR THE USE OF MINIMAL INVASIVE CARDIAC PROCEDURE). STERILE.(B) 1. It should have low profile pods 2. It should have FDA/ European CE (from notified body) certification. 3. Suitable for minimally invasive cardiac surgery.

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HEART POSITIONER (CUP SHAPED)STERILE. (121)(A) 1. Should be suction based. 2. It should be based low profile suction cup 3. It should be compatible with various vogue cardiothoracic retractors. 4. It should have low profile arm designed for better visualization. Should have FDA/ European CE (from notified body) /BIS approved.

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HEART POSITIONER STERILE. (B) 1. Should be on suction based. 2. It should be based low profile 3. It should be compatible with various vogue cardiothoracic retractors. 4. It should have low profile arm designed for better visualization. 5. Should have FDA/ European CE (from notified body) /BIS approved.

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HEART POSITIONER (FOR THE USE OF MINIMAL INVASIVE CARDIAC PROCEDURE). (122)(B) 1. It should be suction based 2. It should have low profile arm designed for better visualization MICAS. 3. Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT FOR AORTIC ARCH GELATIN / COLLAGEN COATED STERILE. (123)(I) 1. It should be coated with gelatin with multiple branches for arch and perfusion. 2. Graft material should have low porosity Dacron (Fabric) 3. Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT FOR AORTIC ARCH GELATIN / COLLAGEN COATED STERILE. (II) 1. It should be coated with collagen with multiple branches for arch and perfusion. 2. Graft material should have low porosity Dacron (Fabric) 3. Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT Y TYPE GELATIN / COLLAGEN COATED STERILE.(124)(A)(I) 1. It should be coated with gelatin. 2. Graft material should have low porosity Dacron (Fabric) 3. Should be provided in sizes of 16x8mm & 14x7mm. 4. Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT Y TYPE GELATIN / COLLAGEN COATED STERILE. (II) 1. It should be coated with collagen. 2. Graft material should have low porosity Dacron (Fabric) 3. Should be provided in sizes of 16x8mm & 14x7mm. 4. Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT STRAIGHT WOVEN STERILE. (B)(I) 1. It should be coated with gelatin or collagen. 2. Graft material should have low porosity Dacron (Fabric). 3. Size 8mm 4. Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT STRAIGHT WOVEN STERILE. (II) 1. It should be coated with gelatin or collagen. 2. Graft material should have low porosity Dacron (Fabric). 3. Size 12 mm 4. Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT STRAIGHT WOVEN STERILE. (III) 1) It should be coated with gelatin or collagen. 2) Graft material should have low porosity Dacron (Fabric). 3) Size 14 mm 4) Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT STRAIGHT WOVEN STERILE. (IV) 1. It should be coated with gelatin or collagen. 2. Graft material should have low porosity Dacron (Fabric). 3. Size 16 mm 4. Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT STRAIGHT WOVEN STERILE. (V) 1) It should be coated with gelatin or collagen. 2) Graft material should have low porosity Dacron (Fabric). 3) Size 18 mm 4) Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT STRAIGHT WOVEN STERILE. (VI) 1. It should be coated with gelatin or collagen. 2. Graft material should have low porosity Dacron (Fabric). 3. Size 20 mm 4. Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT STRAIGHT WOVEN STERILE. (VII) 1) It should be coated with gelatin or collagen. 2) Graft material should have low porosity Dacron (Fabric). 3) Size 22 mm 4) Should have FDA/ European CE (from notified body) /BIS approved.

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VASCULAR GRAFT STRAIGHT WOVEN STERILE. (VIII) 1. It should be coated with gelatin or collagen. 2. Graft material should have low porosity Dacron (Fabric). 3. Size 24 mm 4. Should have FDA/ European CE (from notified body) /BIS approved.

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AXILO FEMORAL RING GRAFT PTFE (125)(A)(I) 1. Material should have EPTFE. 2. It should have rings for kink resistance. 3. Size-6mmx20cm 4. Should have FDA/ European CE (from notified body) /BIS approved.

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AXILO FEMORAL RING GRAFT PTFE (II) 1. Material should have EPTFE. 2. It should have rings for kink resistance. 3. Size-6mmx 40cm 4. Should have FDA/ European CE (from notified body) /BIS approved.

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AXILO FEMORAL RING GRAFT PTFE (III) 1. Material should have EPTFE. 2. It should have rings for kink resistance. 3. Size-6mmx90 cm 4. Should have FDA/ European CE (from notified body) /BIS approved.

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AXILO FEMORAL RING GRAFT PTFE (IV) 1. Material should have EPTFE. 2. It should have rings for kink resistance. 3. Size-7mmx20cm 4. Should have FDA/ European CE (from notified body) /BIS approved.

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AXILO FEMORAL RING GRAFT PTFE (V) 1. Material should have EPTFE. 2. It should have rings for kink resistance. 3. Size-7 mmx 40cm 4. Should have FDA/ European CE (from notified body) /BIS approved.

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AXILO FEMORAL RING GRAFT PTFE (VI) 1. Material should have EPTFE. 2. It should have rings for kink resistance. 3. Size-7mmx90 cm 4. Should have FDA/ European CE (from notified body) /BIS approved.

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AXILO FEMORAL RING GRAFT PTFE (VII) 1. Material should have EPTFE. 2. It should have rings for kink resistance. 3. Size-8mmx20cm 4. Should have FDA/ European CE (from notified body) /BIS approved.

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AXILO FEMORAL RING GRAFT PTFE (VIII) 1. Material should have EPTFE. 2. It should have rings for kink resistance. 3. Size-8mmx40cm 4. Should have FDA/ European CE (from notified body) /BIS approved.

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AXILO FEMORAL RING GRAFT PTFE (IX) 1. Material should have EPTFE. 2. It should have rings for kink resistance. 3. Size-8mmx90 cm 4. Should have FDA/ European CE (from notified body) /BIS approved.

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AXILO FEMORAL RING GRAFT PTFE, THIN WALL. STERILE. (126)(B)(I) 1. It should be in various sizes and length6mm x 70 cm 2. Material should have thin wall PTFE.-. 3. It should have rings for kink resistance. 4. Should have FDA/ European CE (from notified body) /BIS approved.

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AXILO FEMORAL RING GRAFT PTFE, THIN WALL. STERILE. (II) 1. It should be in various sizes and length6mm x 90 cm 2. Material should have thin wall PTFE.-. 3. It should have rings for kink resistance. 4. Should have FDA/ European CE (from notified body) /BIS approved.

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AXILO FEMORAL RING GRAFT PTFE, THIN WALL. STERILE. (III) 1. It should be in various sizes and length7mm x 70 cm 2. Material should have thin wall PTFE.-. 3. It should have rings for kink resistance. 4. Should have FDA/ European CE (from notified body) /BIS approved.

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AXILO FEMORAL RING GRAFT PTFE, THIN WALL. STERILE. (IV) 1. It should be in various sizes and length7mm x 90 cm 2. Material should have thin wall PTFE.-. 3. It should have rings for kink resistance. 4. Should have FDA/ European CE (from notified body) /BIS approved.

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AXILO FEMORAL RING GRAFT PTFE, THIN WALL. STERILE. (V) 1. It should be in various sizes and length8mm x 70 cm 2. Material should have thin wall PTFE.-. 3. It should have rings for kink resistance. 4. Should have FDA/ European CE (from notified body) /BIS approved.

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AXILO FEMORAL RING GRAFT PTFE, THIN WALL. STERILE. (VI) 1. It should be in various sizes and length8mm x 90 cm 2. Material should have thin wall PTFE.-. 3. It should have rings for kink resistance. 4. Should have FDA/ European CE (from notified body) /BIS approved.

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AXILO FEMORAL RING GRAFT PTFE,THIN WALL COATED WITH CARBON. STERILE. (127)(C)(I) 1. It should be Size 7& 8mmx70,90 cm 2. Material should have thin wall with carbon coated PTFE. 3. It should have rings for kink resistance. 4. Should have FDA/ European CE (from notified body) /BIS approved.

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AXILO FEMORAL RING GRAFT PTFE,THIN WALL COATED WITH CARBON. STERILE. (II) 1. It should be Size 7& 8mmx70,90 cm 2. Material should have thin wall with carbon coated PTFE. 3. It should have rings for kink resistance. 4. Should have FDA/ European CE (from notified body) /BIS approved.

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AXILO FEMORAL RING GRAFT PTFE,THIN WALL COATED WITH CARBON. STERILE. (III) 1. It should be Size 7& 8mmx70,90 cm 2. Material should have thin wall with carbon coated PTFE. 3. It should have rings for kink resistance. 4. Should have FDA/ European CE (from notified body) /BIS approved.

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AXILO FEMORAL RING GRAFT PTFE,THIN WALL COATED WITH CARBON. STERILE. (IV) 1. It should be Size 7& 8mmx70,90 cm 2. Material should have thin wall with carbon coated PTFE. 3. It should have rings for kink resistance. 4. Should have FDA/ European CE (from notified body) /BIS approved.

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INTRODUCER Sheath (128)(I) Sheath 8.5 F, Dilator, sleeve, Introducer Needle 18GX7cm Guidewire 0.035±0.003” J tip, Scalpel, syringe 5 ml Should have FDA/ European CE (from notified body) /BIS approved.

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INTRODUCER Sheath Size8.5F with sleeve (II) Introducer Needle 18G, Dilator, sheath 10F 11cm syringe Guidewire 0.035±0.003” J tip, Scalpel, syringe 3 ml Should have FDA/ European CE (from notified body) /BIS approved.

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Introducer Sheath 10 F (III) Introducer Needle 18G, Dilator, sheath 8F 11cm syringe Guidewire 0.035±0.003” J tip, Scalpel, syringe 3 ml Should have FDA/ European CE (from notified body) /BIS approved.

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Micropore Silicon Tape 1 Inch (129)(I) Rayon and Polyester Fiber with resin Copolyester film, silicone release coating and bi-directional tear-ability. It is coated with a silicone gel adhesive which has a spring action and low surface tension allowing it to bond quickly at application with the adhesion remaining constant with time. Micropore Silicon tape Size 1 Inch x 5.5 Yd It Should have BIS/USFDA/European CE (Form notified body) certification.

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Micropore Silicon Tape 2 Inch (II) Rayon and Polyester Fiber with resin Copolyester film, silicone release coating and bi-directional tear-ability. It is coated with a silicone gel adhesive which has a spring action and low surface tension allowing it to bond quickly at application with the adhesion remaining constant with time. Micropore Silicon tape Size 2 Inch x 5.5 Yd It Should have BIS/USFDA/European CE (Form notified body) certification

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Cap for male leurs (130) Alcohol-containing caps that twist onto distal end of I.V tubing and other male luer devices for disinfection and protection. Each cap contains 70% isopropyl alcohol (IPA) which bathes the surface of the port and disinfects it in 1 minute and protects ports for up to 7 days if not removed. Disinfecting port protector caps with 70% IPA for distal end of IV tubing and other male luer devices It Should have BIS/USFDA/European CE (Form notified body) certification.

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Cap for Female leurs Alcohol-containing caps that twist onto distal end of I.V tubing and other male luer devices for disinfection and protection. Each cap contains 70% isopropyl alcohol (IPA) which bathes the surface of the port and disinfects it in 1 minute and protects ports for up to 7 days if not removed. Disinfecting port protector caps with 70% IPA for distal end of IV tubing and other male luer devices It Should have BIS/USFDA/European CE (Form notified body) certification.

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way-3 stop cock with extension line 200cm (131)(I) 200 cm extension tube should be attached in male port of 3-way stop cock. Male luer port should remain free of extension tube It Should have BIS/USFDA/European CE (Form notified body) certification.

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way-3 stop cock with extension line 150cm (II) 150 cm extension tube should be attached in male port of 3-way stop cock. Male luer port should remain free of extension tube It Should have BIS/USFDA/European CE (Form notified body) certification.

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way-3 stop cock with extension line 100cm (III) 100 cm extension tube should be attached in male port of 3-way stop cock. Male luer port should remain free of extension tube It Should have BIS/USFDA/European CE (Form notified body) certification.

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way-3 stop cock with extension line 50cm (IV) 50 cm extension tube shoulb be attached in male port of 3-way stop cock. Male luer port should remain free of extension tube It Should have BIS/USFDA/European CE (Form notified body) certification.

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Pressure Infusion Bag (132) Pressure infusion clear cuff bag 500/ 1000ml size for fast delivery of fluids for use in pre post-operative care. Unit should have a pressure gauge, convenient IV pole mounting having durable construction. It should have clear sleeve around bag to provide a visible window to see what fluid is being pressurized. It should come with a pound fitted efficient hand bulb to make easy inflation with maximum pressure protection at 300mm of Hg It Should have BIS/USFDA/European CE (Form notified body) certification.

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Chest drain suction control 1000 ml Negative suction drain bottle (133) seal system with mechanical one way valve. Scheffier’s one way valve is present. Low opening pressure of -1cm H2O Flexible and able to milk manual suction bulb included. Length 150cm includes three sized of the connector Sterile and closed drainage system 1000ml fluid holding capacity can be drained out using in built drainage tap. Negative suction source can be connected to air vent port with inbuilt suction regulator between -5to -40cm H2O Check presence of air bubbles to diagnose a persistent air leak broncho pleural fistula. Detection of size of air- leak. The compact and light weight design of chest drain facilities early mobilization of patients The device does not have to be kept upreight at all times. It may even be lifted higher then the patients. A shoulder sing is provided to enhance patient comfort when mobilizing. It Should have BIS/USFDA/European CE (Form notified body) certification.

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Surgical clipper blade (134) Disposable surgical clipper blade with ribbed design to remove all types of Surgical Procedure, Body Hair , head hair , including sensitive area of the body with single blade (dry and wet).one blade should stationery thats touch skin and cuts away from the skin positioning with width of 35mm to 40mm. equipment should have a run time of around 150-180 minutes on a 220-250 minutie recharge

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Antimicrobial Incise Drape Medium (135) Incisde drape made up of Polyester film with an acrylic adhesive that contains a complex of iodoform(N- vinyl 2 pyrrolidine) with a iodine concentration of 0.090 to 0.100 mg Iodine/cm2. Film should be breathable and conformable to skin, compatible with Povidone and CHG skin preps. Iodine from the drape should be present in the deepest skin layers (atleat 900 to 1000 microns depth) where hair folices exist apart from killing microbes on skin layer. Size range from 30-35cmX30-35cm

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Antimicrobial Incise Drape Large. (136) Incisde drape made up of Polyester film with an acrylic adhesive that contains a complex of iodoform(N- vinyl 2 pyrrolidine) with a iodine concentration of 0.090 to 0.100 mg Iodine/cm2. Film should be breathable and conformable to skin, compatible with Povidone and CHG skin preps. Iodine from the drape should be present in the deepest skin layers (atleat 900 to 1000 microns depth) where hair folices exist apart from killing microbes on skin layer. Size range from 50-55cmX40-45cm

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Chemical Integrator (137) Moving front Chemical integrators to verify all perimeters of steam sterilization together i.e. Time, Temperature and Quality of steam. Read out indicates Accept or Reject after processing. Individually packaged and labeled with lot number and expiration date on each roll. Vibrant color branding at the flip side to quickly locate the CI in a pack/set. "• Should be compliant to BS/ EN/ ISO 11140-1: 2005

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Super Rapid Biological Indicator for Steam (139) Super Rapid BI: Super Rapid readout biological indicators for steam sterilization containing a standardized, viable population of Bacillus stearothermophilus spores. The indicator detects the presence of viable spores by the production of fluorescence with in 25-30 mins. Designed and certified as per ISO 11138 and EN 866. Should be compatible with the pre Vacuum cycle of 132°C to 135°C. Should be compliant to ISO 11138-1:2006(en) Part 1 and ISO 11138-1:2006(en) Part 3 .

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Full Body Adult Patient Warming Blanket (140) Full Body Adult Patient Warming Blanket should Uniform perforation pattern across the blanket surface ensures even convective warming with resealable hose ports for to adapt blanket to Pre OP, Post OP and ICU care. It should be latex free with superior top layer having insulating and unique air channels for even heat distribution.It should be non-conductive ,non-irritable and must confirm to flammability standards. Size - 212X990CM ± 5cm.

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Full Body Patient Warming Blanket pediatric (141) Full Body Paediatric Patient Warming Blanket should Uniform perforation pattern across the blanket surface ensures even convective warming with resealable hose ports for to adapt blanket to Pre OP, Post OP and ICU care. It should be latex free with superior top layer having insulating and unique air channels for even heat distribution.It should be non-conductive ,non-irritable and must confirm to flammability standards. Size - 152X91CM ± 5cm.

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