Corazon Locsin Montelibano Memorial Regional Hospital doh R6 Tender

Description Item Description Abc Unit Quantity 1 Sheath Fluid-fus (20 Liters) 800,000.00 Pack 20.00 2 Cleaning Fluid Ii 500ml 191,044.00 Bottle 28.00 3 Cleaning Fluid (urine Sediment Detergent, 500ml) 54,584.00 Bottle 8.00 4 Fe Focus B Ii (urine Analyzer Reagent, 125ml) 248,472.00 Bottle 28.00 5 Negative Control (urine Analyzer) 125ml 141,984.00 Bottle 16.00 6 Positive Control Level 3 (urine Analyzer) 125ml 141,984.00 Bottle 16.00 7 Urinalysis Control Qc (positive) 4x8ml/kit 894,240.00 Kit 184.00 8 Urinalysis Control Qc (negative) 4x8ml/kit 894,240.00 Kit 184.00 9 Urine Strips 14 Ca Ii (100's/bot) 648,000.00 Bottle 360.00 10 Fe Calibrator Ii (for Urine Analyzer) 125ml 70,992.00 Bottle 8.00 Terms Of Reference For Procurement Of Reagents For Automated Urinalysis (revised July 18,2023) This Is Lot Bid The Supplier Awarded To Supply The Reagents Shall Adhere To The Terms Of Reference Stated Below: 1. Provide For Free The Following Equipment Necessary For The Testing, Data Processing And Analysis, Generation Of Results, And Efficient System Operation: 1a. A Heavy Duty Fully Automated And Incredible Bench Type Urine Analyzer That Provides The Most Comprehensive 43 Report Parameters And 2 Research Parameters Results. Integrated With Sheath Flow Technology, High-speed Photograph Technology (2000 Frames Imagex400times Magnification) And Artificial Intelligent Identification. Additional Analyzer Features Shall Include: -analytical System Capable Of Detecting Twenty-five (25) Formed Elements In The Urine (e.g., Red Cells, Leukocytes, Crystals, Casts, Epithelial Cells, Bacteria, Yeast, Red Blood Cell Morphology, Etc.) Thru Classical Flow Imaging Analysis Technology. Included For Identifications Are The Particles Sub-classification After High Value Reference For Clinical Diagnosis. -the Analytical System, Likewise, Is Capable Of Detecting Fourteen (14) Chemical Analytes Plus 4 Physical Parameters In Urine (e.g., Glucose, Protein, Microalbumin, Ketones, Calcium, Ascorbic Acid, Nitrite, Leukocyte, Blood, Creatinine, Bilirubin, Urobilinogen, Etc.) And Determining Urine Physical Properties (e.g., Ph And Specific Gravity) Thru Photoelectric Colorimetry. Thus, Integrating Physical, Chemical And Formed Element Analysis. -complete Quality Assurance System -complete Calibrator, Quality Control, Strip And Reagent -throughput Of At Least 120 Samples Per Hour As Hybrid Mode/formed Element Mode And At Least 240 Tests/hour As Chemistry Mode; Walk-away System With Continuous Loading; - Can Read Samples With Volume Less Than 3ml To Formed Elements Mode And 1.5 Ml To Chemistry Mode; Bar Code Reading Capable; High Precision Sipping And Dripping System With Aspiration Volume Of 2.2 Ml To Formed Elements And 0.4 Ml To Chemistry Mode; Variable Power Requirement 100-240v 50hz/60hz - Operation Temp. 10-30°c - Connection Capability To Lis And/or His - Dimension Of Machine Shall Fit In To Allotted Space In The Clinical Microscopy Section, Not Exceeding 900mm (l) X 1600mm (w) X 600mm (h). -acceptable Total Analytical Error (tae) For Measurable Parameters/analytes; Tae For Each Parameter/analyte Shall Be Within Set Standards Or As Set By Manufacturer; Tae Shall Be Determined By Equipment Performance Verification Or Validation Conducted In Conjunction With Laboratory Staff Employing Acceptable Method - Preferably Brand New, But Equipment Not More Than 3 Years Old Is Acceptable 1b. Compatible Ups For The Analyzer 1c. Preferably With Corresponding Computer Hardware And Software Integrated With The Analyzer 2. Provide For Free The Installation, Regular Preventive Maintenance And Calibration Of Equipment, Replacement Of Parts Or Units Duly Coordinated With Concerned Laboratory Staff And Efm Personnel. 3. Provide For Free The Training And Re-training Of Laboratory Staff To Make Them Competent To Operate The Equipment. 4. Has The Capacity To Upgrade The Equipment Provided When Necessary Or When Need Arises Upon Request By The End User Without Additional Cost To Procured Reagents. 5. The Moa Shall Cover A Period Of 3 Months With Added Stipulation For Extended Use Of Machine For Free In Case The Reagents Will Not Be Consumed Within 3 Months. 6. Ensure Compliance With Scheduled Preventive Maintenance And Calibration Of Equipment. 7. Ensure Prompt Response By Designate Engineer/s Within 24 Hours For Correction Of Equipment Failure Or Malfunction. 8. Reimburse All Examinations That Are Sent Out Related To Equipment Failure Or Malfunction. 9. Replenish Consumed Reagents And Other Consumables Incidental To Repeated Test Runs Due To Equipment Failure, Malfunction Or Trial Runs During Training/re-training. 10. Assures Replacement Of Unused Reagents And Consumables (delivered Within 3months Of Expiration Date) Before Expiration. Longer Expiration Date, Specifically 1-2 Years For All Reagents Is A Must. 11. Assures Replacement Of Reagents And Consumables With 1-month Remaining Shelf Life Before The Expiration Date. 12. Provide For Free Reagents And Consumables And Service Assistance For Equipment Performance Verification Or Validation 13. Will Shoulder Connection Fee To Lis Of Choice Of End-user And/or His. 14. The Product Carried Must Covered By A Current Certificate Of Product Registration Or, In The Absence Of The Former, Proof Of Renewal Or Updated Certificate Of Exemption Issued By Philippine Fda. 15. Manufacturing Of Reagents And Equipment Are Covered By Relevant Iso Certification Or Quality Certification Of Similar Nature 16. Supplier/distributor Is Preferably, But Not Necessarily, Iso 9001:2015 Certified 17. Provide Updated Material Safety Data Sheet (msds) For Chemical Reagents Upon Delivery Of Items. Total Abc 4,085,540.00