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Costs
EMD
₹ 22,93,217Document Cost
₹ 50,000Tender Fee
₹ 5,900
Summary
Design Installation Testing And Commissioning Of Mg And Allied Works In Advanced Trauma Center
Description
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Contact
Tender Id
2025_CEPW_133679_1Tender No
Bid No 65 dated 23-01-2025Tender Authority
Public Works Department ViewPurchaser Address
-Website
http://https://pwdpunjab.gov.in/
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BOQ Items
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S/1/T/C of Fully Automatic Oxygen Control Panel, as per HTM-2022/02-01 of UK NFPA99C of USA as per enclosed technical specifications - (Imported)
Gas Manifold should be fully automatic, self- shifting to reserve bank on exhaustion of the service bank without interruption of gas delivery to the system. Critical connections should be gas specific, non- interchangeable and should be designed to eliminate gas supply error. The manifold control system should supply a flow of 1500 L/ Min at 50 psi. The dual line regulator/single vent Medical Gas Manifold control unit should include right and left header bars and pigtails for the appropriate medical gas. The installed system should automatically switch over to the reserve bank when the primary bank is depleted. When the depleted cylinders are replaced with full cylinders the system should automatically reset itself in preparation for the next bank change. The primary side bank in use and the remaining side bank on reserve. This designation should automatically change from left to right and right to left as each bank is depleted and, in turn, refitted with full gas cylinders.
The LED indicator should show a depleted bank by turning red. A buzzer should also sound to indicate an empty bank. When the system is reset by replacing the depleted cylinders, the indicator should turn green and also silence the buzzer. If the manifold is connected to the health care facility's central alarm system that should also indicate that the bank was depleted and, in turn, was reset. The only manual activity Medical gas Manifold requires is the changing of the depleted cylinders. When a bank is depleted, Manifold should automatically switch to the fresh bank, delivering an uninterrupted gas supply to the health care facility. Changeover is performed by solenoid valves contained in the control cabinet. In the event of an electrical power failure, both solenoid valves should automatically open to provide an uninterrupted gas flow. Under normal operating conditions, the gas should leave the high pressure cylinders through the pigtails into the header bars.
The pigtails should have on-way Valves (check valves) to allow the replacement of depleted cylinders with out gas pressure back-flow into the remaining depleted cylinders on that bank. In the event a safety relief device on an individual cylinder should activate or a pigtail should leak excessively, the local check vale should also prevent loss of gas from the rest of the cylinders on that bank.
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The gas should flows through the manually operated shutoff valve into the primary regulator. This regulator should reduce the high cylinder pressure to an intermediate pressure. The intermediate pressure gas flows through the solenoid valve to the line regulator for its final (Line) pressure reduction for use in the health care facility. Two line pressure regulators should be installed in parallel, and each should be capable of maintaining a constant dynamic delivery pressure at the maximum designed flow rate of the system.
The solenoid valve should be the key to the automatic mechanism the manifold. This component ensures that the flow of gas is not interrupted and the pressure does not fluctuate during normal operation. When the operating bank pressure falls to a predetermined level, which is controlled by the preset pressure switches (high and low) , the switches should activate the solenoids to switch to the fresh (reserve) cylinder bank.
The manifold control cabinet should have three means of giving continuous information on the system status: first pressure gauges to indicate the bank pressure and the delivery pressure: second six indicator LEDs, two green that indicate which cylinders is in use, two yellow for Reserve Ready and two red that indicate a bank is now depleted: third, a loud audible buzzer gives an alarm when either or both banks are depleted.
The six indicators should controlled by sensing the bank pressure. Replacing the depleted cylinders on the empty bank resets the system, changing the indicator from red to yellow. At the same time the yellow LED should change to green to go form Reserve Ready to In Service. LEDs should show red prior to initial pressurization or whenever both cylinder banks are below the preset value.
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S/1/T/C of Oxygen Manifold Emergency for 12 Cylinders, as per enclosed technical specifications -(indian) (without cylinder)
The oxygen cylinder manifold should comprise of two cylinder Banks which can accommodate 6 cylinders in each Bank (means 6+6) complete with copper tail pipes with bull nose fittings of RH External threading suitable for cylinder valves conforming to IS 3234 (Oxygen service) and Cylinder support system.
Manifold should be suitable to withstand a pressure of 140 Kg/cm2, along with high pressure copper annealed tail pipes with Brass adapter suitable for Oxygen Cylinders and manifold.
Top frame comprising of high pressure copper pipes of size 1/2" I. D. x 15swg with high pressure brass fittings made of high tensile brass and connections through non- return valves.
High pressure copper tail pipes, made of high pressure copper pipe of size 1/4" I. D. x 15 swg.
The middle and bottom frame to be provided to fit both round and flat bottom cylinders safely. The manifold should be tested (hydraulically) at 250kg I em sq.
The copper tail pipes are fitted to the individual non return valves of the cylinder manifold for easy removal of cylinders without disturbance to system operation.
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S/1/T/C of Oxygen Outlets with matching probes, as per
HTM-2022/02-01 of UK NFPA99C of USA as per enclosed technical specifications - (Imported) Oxygen, Air-4 &Air-7, N20, WAGD/AGSS
Vacuum, Surface mount, non interchangeable, self sealing outlets, outlets should consist of a roughing in assembly and a finishing assembly. A non removable positive- pin keying arrangement for each specific gas service. Installed in the mounting box a fully assembled brass secondary check valve.
Design of outlet should be such that it should have 100% metal construction for corrosion resistance fire safety & push button mechanism for quick release of adaptor. The secondary check valve automatically should form a positive seal to prevent a gas flow when the finishing assembly is removed. The secondary check valve to include 7" (17.78cm) of 1/2" Type K copper tubing with a label affixed which identifies the specific gas by name and colour.
A plastic cap inserted at the end of the inlet tube. Rotation of the inlet tube should allow gas connection from the top or bottom. the finishing assembly should consists of a die cast chrome plated cover plate , a machined brass housing for the primary check valve, and a positive -pin keying device to prevent accidental installation into a roughing in assembly of a dismal gas. The finishing assembly should incorporate a double seal arrangement which automatically engages when a hose adapter or patient treatment device is removed from the outlet. The design of the outlet should be such that if can be easily repaired without disassembly of the outlet.The finishing assembly should have a colour coded (specific gas) keying disc to prevent connection of hose adapters or patient treatment device to the wrong gas service. The primary check allows absolutely no gas flow to take place until the keying devices are engaged. It should be manufactured in accordance with all applicable NFPA and CGA standards. The locking device should be in the probe instead of gas outlet.,Matching probe for outlets- Imported as per NFPA -99 I HTM 02-01 UL Listed ICE Marked Matching probes
to the gas outlet mentioned above. That is adapter for Oxygen & vacuum. Each adapter should have suitable barb or threads so that it can be connected to tube or flow meter /suction regulator. Adapter should have clear gas service embossed on it.
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S/1/T/C of Oxygen Flowmeter with Humidifier Bottle, as per enclosed technical specifications - (Imported) for critical area The graduated scale should have an oval shape which allows a "lens effect" get the scale values easy-reading in any condition of use.
On/OFF switch button of green and red color which allows the operator to quickly identify lock and reactivate the flowmeter gas supply and also keepsn the previous flow preset value unchanged. It should have ADJUSTING KNOB WITH PUSH&LOCK SYSTEM: it keep locked the pre-set flow value. To adjust the flow pull the knob, set the flow value you need to deliver to the patient and push the knob to lock the selected value.
The flowmeter should have an integrated pressure reducer for the stabilization of supplied pressure at 2.8bar, to guarantee the flow accuracy of the device. The flowmeter should be useable in any area of hospital with different pressure from the plants and it is not necessary to calibrate it.
The outlet nipple should have a double thread interchangeable through slide and at one time one thread is visible and second thread should be stored in flowmeter body . The flowmeter should not have less then 50 mm adjusting knob with soft grip inserts for easy handling. The humidifier should be completely made of polycarbonate / polypropylene and should be autoclavable at 121 °C for 15 min. For the inlet connection it should have some snap inserts, identified with color-code, with different threads to be chosen by the end user. An ergonomic and big size rotating nut which allows easy connecting and disconnecting the humidifier to the oxygen supply device. The 360° rolling positioning hose connector ø 6÷9 mm allowing an easy use of the humidifier. The bottle should have hollow shape, besides being a design unique element, offers the operator an easy and safe handling. The humidifier should have an integrated relief valve
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S/1/T/C of Oxygen Flowmeter with Humidifier Bottle, as per enclosed technical specifications - (Imported) for other area
Brass body chrome plated Flowmeter with colour coding to match with the gas being used. The housing should be made of polypropylene to ensure high durability. The flow range should be 0-15 LPM. The Flowmeter should be fitted with matching adaptor (probe) for Oxygen Gas Outlet Point. The Flow meter should be CE marked/UL Listed.
Humidifier bottle should be compatible with Oxygen Flowmeter & it should be reusable type. The bottle should be shatterproof & made of polypropylene. Metal components of humidifier bottle should be made of brass with anti-corrosion nickel plating.
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MEDICAL NITROUS OXIDE SYSTEM
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S/1/T/C of N20 Manifold with 8 Nos. pigtail pipes for 4+4 cylinders and Non-return valves, as per enclosed technical specifications -(indian) (without cylinder)
The N20 cylinder manifold should comprise of two cylinder Banks which can accommodate 4 cylinders in each Bank (means 4+4) for cylinder valves conforming to IS 3234 (N20 service) complete with copper tail pipes with fittings.
Manifold should be suitable to withstand a pressure of 140 Kg/cm2, along with high pressure copper annealed tail pipes with Brass adapter suitable for Nitrous Cylinders and manifold.
Top frame comprising of high pressure copper pipes of size 1/2" I. D. x 15swg with high pressure brass fittings made of high tensile brass and connections through non- return valves.
High pressure copper tail pipes, made of high pressure copper pipe of size 1/4" I. D. x 15 swg.
The middle and bottom frame to be provided to fit both round and flat bottom cylinders safely. The manifold should be tested (hydraulically) at 250kg I em sq.
The copper tail pipes are fitted to the individual non return valves of the cylinder manifold for easy removal of cylinders without disturbance to system operation.
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S/1/T/C of Fully Automatic N20 Control Panel, as per HTM-2022/02-01 of UKINFPA99C of USA as per enclosed technical specifications - (Imported)
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S/I/T/C of Nitrous Oxide Manifold Emergency for 2 Cylinders, with high pressure Regulator,NRV,tailpipes etc. as per enclosed technical specifications - (Indian)
(without cylinder)
The N20 cylinder manifold should comprise of two cylinder Banks which can accommodate 1cylinder in each Bank (means 1+1) complete with copper tail pipes with bull nose fittings of RH External threading suitable for cylinder valves conforming to IS 3234 (N20service) and Cylinder support system.
Manifold should be suitable to withstand a pressure of 140 Kg/cm2, along with high pressure copper annealed tail pipes with Brass adapter suitable for N20 Cylinders and manifold.
Top frame comprising of high pressure copper pipes of size 1/2" I. D. x 15swg with high pressure brass fittings made of high tensile brass and connections through non- return valves.
High pressure copper tail pipes, made of high pressure copper pipe of size 1/4" I. D. x 15 swg.
The middle and bottom frame to be provided to fit both round and flat bottom cylinders safely. The manifold should be tested (hydraulically) at 250kg I em sq.
The copper tail pipes are fitted to the individual non return valves of the cylinder manifold for easy removal of cylinders without disturbance to system operation.
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S/1/T/C of N20 Outlets with matching probes, as per
HTM-2022/02-01 of UKINFPA99C of USA as per enclosed technical specifications - (Imported)
Surface mount, non interchangeable, self sealing outlets, outlets should consist of a roughing in assembly and a finishing assembly. A non removable positive- pin keying arrangement for each specific gas service. Installed in the mounting box a fully assembled brass secondary check valve.
Design of outlet should be such that it should have 100% metal construction for corrosion resistance fire safety & push button mechanism for quick release of adaptor. The secondary check valve automatically should form a positive seal to prevent a gas flow when the finishing assembly is removed. The secondary check valve to include 7" (17.78cm) of 1/2" Type K copper tubing with a label affixed which identifies the specific gas by name and colour.
The finishing assembly should have a colour coded (specific gas) keying disc to prevent connection of hose adapters or patient treatment device to the wrong gas service. The primary check allows absolutely no gas flow to take place until the keying devices are engaged. It should be manufactured in accordance with all applicable NFPA and CGA standards. The locking device should be in the probe instead of gas outlet.
Matching probe for outlets- Imported as per NFPA -99 I HTM 02-01 UL Listed ICE Marked Matching probes
to the gas outlet mentioned above. That is adapter for Oxygen & vacuum. Each adapter should have suitable barb or threads so that it can be connected to tube or flow meter /suction regulator. Adapter should have clear gas service embossed on it.
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MEDICAL COMPRESSED AIR SYSTEM
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S/1/T/C of Duplex Compressor complete with Compressed air plant complete along with electrical control panel as per tender specifications fulfilling HTM 2022-02-01I NFPA99C as per enclosed technical specifications -(imported)
a) The system should be designed to deliver total plant capacity 80 scfm to the hospital (running +standby )and associated equipment, one vertical ASME Tank and one control panel. The entire system including the receiver should be mounted on a common structural steel stack base. The only field connections required would be system intake, exhaust and power connection at the control panel. All components should be completely prepiped and pre-wired to single-point service connections. All interconnecting piping and wiring should be completed and operationally tested at the site of manufacturer.
b)The medical air compressors should be of screw/scroll technology air-cooled design. Connecting rod and bearings should be packed with lifetime lubrication and sealed.
c) Each compressor should be belt driven by a suitable HP, 3 phase, 50 cycle, 415 volt, ODP NEMA construction motor. Slide bases for convenient belt tension adjustment and totally enclosed OSHA approved belt guards should be provided.
d) Each air compressor should have a capacity of 40 scfm at 100 PSIG.
e) The system should include individual compressor inline intake filters, discharge check valves of bronze construction, safety relief valves, bronze intake and discharge flexible connectors, solenoid unloaders, isolation valves, air cooled after coolers for each compressor, high discharge temperature shut down switches on each cylinder, pressure control switches, as well as copper tubing with shut-off cock for gauge and switches. The system should include a 120 gallon. Pressure storage tank of ASME construction rated for 200-PSI MWP service. The tank should be equipped with a pressure gauge, safety relief valve, 3-way by-pass; gauge glass and automatic electronic tank drain with manual override. The inside of the tank should be coated for rust protection with a two component coating which provides a hard, durable lining. Provide spring vibration isolators for each compressor.
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f)The system should include a UL listed control panel in a NEMA 12 enclosure with the following accessories for each pump:
g) Externally operable fusible disconnect with door interlock, control circuit transformer with fused primary and secondary coils, H-0-A switch, magnetic starter with 3 leg overload protection, hour meter, motor running light. Provide the panel with a multiple position selector switch for selection of normal operation (automatic alternation) or manual selection of lead and lag pumps if one of the pumps is taken out of service due to scheduled maintenance. Provide audible and visual local alarm (complete with indicating lights and individual sets of auxiliary contacts wired to the terminal strip for remote alarm indication) for the following: compressor temperature malfunction and reserve compressor in use.
Provide manual reset for thermal malfunction shutdown. All control and alarm functions should remain energized while any compressor in the system remains electrically on-line. The lag compressor should be able to start automatically if the lead compressor fails to operate.
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STANDARD BILL OF MATERIAL FOR DUPLEX
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DESCRIPTION
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Duplex
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Oil-Less Compressor = 2,Belt Guard = 2,Electric Motor = 2,High Air Temperature Switch = 2,Air Receiver ( ASM E Rated) = 1,Control Pressure Switch = 2,Three-Valve By pass = 1,Sight-Gauge Glass = 1,Pressure Gauge = 1,Pressure Relief Valve = 1,Automatic Tank Drain = 1,Electrical Control Panel = 1,NEMA 12 Enclosure = 1,Power Distribution Block = 1,Combination Motor Starters with Circuit Breaker Disconnects = ,Automatic Alternation = 1,Running Lights = 2,Hour Meters = 2,Control Transformer = 2,Hand-Off Automatic switch = 2,High-Air Temperature Light with contacts = 2,Lag On Alarm with Horn, Light & contacts = 1,Interconnecting piping = 1lot,Compressors Isolating Valve = 2,Check Valve = 2,Compressor Inlet flex connectors (installed) = 2,Compressor Discharge Flex Connectors (installed) = 2,System Flex Connector (shipped loose) = 2,Vibration Dampeners (Shipped Loose) = 1set
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S/1/T/C of Air-4 Bar Outlets with matching probes, as per
HTM-2022/02-01 of UKINFPA99C of USA as per enclosed technical specifications - (Imported)
Surface mount, non interchangeable, self sealing outlets, outlets should consist of a roughing in assembly and a finishing assembly. A non removable positive- pin keying arrangement for each specific gas service. Installed in the mounting box a fully assembled brass secondary check valve.
Design of outlet should be such that it should have 100% metal construction for corrosion resistance fire safety & push button mechanism for quick release of adaptor. The secondary check valve automatically should form a positive seal to prevent a gas flow when the finishing assembly is removed. The secondary check valve to include 7" (17.78cm) of 1/2" Type K copper tubing with a label affixed which identifies the specific gas by name and colour.
A plastic cap inserted at the end of the inlet tube. Rotation of the inlet tube should allow gas connection from the top or bottom. the finishing assembly should consists of a die cast chrome plated cover plate , a machined brass housing for the primary check valve, and a positive -pin keying device to prevent accidental installation into a roughing in assembly of a dismal gas. The finishing assembly should incorporate a double seal arrangement which automatically engages when a hose adapter or patient treatment device is removed from the outlet. The design of the outlet should be such that if can be easily repaired without disassembly of the outlet.
The finishing assembly should have a colour coded (specific gas) keying disc to prevent connection of hose adapters or patient treatment device to the wrong gas service. The primary check allows absolutely no gas flow to take place until the keying devices are engaged. It should be manufactured in accordance with all applicable NFPA and CGA standards. The locking device should be in the probe instead of gas outlet.
Matching probe for outlets- Imported as per NFPA -99 I HTM 02-01 UL Listed ICE Marked Matching probes
to the gas outlet mentioned above. That is adapter for Oxygen & vacuum. Each adapter should have suitable barb or threads so that it can be connected to tube or flow meter /suction regulator. Adapter should have clear gas service embossed on it..
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SIIITIC of Air-7 Bar Outlets with matching probes, as per HTM-2022102-01 of UKINFPA99C of USA as per enclosed technical specifications - (Imported)
Surface mount, non interchangeable, self sealing outlets, outlets should consist of a roughing in assembly and a finishing assembly. A non removable positive- pin keying arrangement for each specific gas service. Installed in the mounting box a fully assembled brass secondary check valve.
Design of outlet should be such that it should have 100% metal construction for corrosion resistance fire safety & push button mechanism for quick release of adaptor. The secondary check valve automatically should form a positive seal to prevent a gas flow when the finishing assembly is removed. The secondary check valve to include 7" (17.78cm) of 1/2" Type K copper tubing with a label affixed which identifies the specific gas by name and colour.
A plastic cap inserted at the end of the inlet tube. Rotation of the inlet tube should allow gas connection from the top or bottom. the finishing assembly should consists of a die cast chrome plated cover plate , a machined brass housing for the primary check valve, and a positive -pin keying device to prevent accidental installation into a roughing in assembly of a dismal gas. The finishing assembly should incorporate a double seal arrangement which automatically engages when a hose adapter or patient treatment device is removed from the outlet. The design of the outlet should be such that if can be easily repaired without disassembly of the outlet.
The finishing assembly should have a colour coded (specific gas) keying disc to prevent connection of hose adapters or patient treatment device to the wrong gas service. The primary check allows absolutely no gas flow to take place until the keying devices are engaged. It should be manufactured in accordance with all applicable NFPA and CGA standards. The locking device should be in the probe instead of gas outlet
Matching probe for outlets- Imported as per NFPA -99 I HTM 02-01 UL Listed ICE Marked Matching probes
to the gas outlet mentioned above. That is adapter for Oxygen & vacuum. Each adapter should have suitable barb or threads so that it can be connected to tube or flow meter /suction regulator. Adapter should have clear gas service embossed on it.
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MEDICAL VACCUM CENTRAL SYSTEM
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SIIITIC of Duplex Vacuum central system with duplex pump only complete with electrical control panel as per tender specifications as per HTM 2022-02-01I NFPA99C as per enclosed technical specifications(imported)
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Duplex VACUUM (SUCTION) SUPPLY SYSTEM- as per NFPA-99 std I HTM -2022102-01 (imported)
The system should be designed to deliver total plant capacity 4200 LPM ( running + standby ) to the hospital .
The Oil Lubricated Rotary Vane Medical vacuum System should provide superior performance with minimal maintenance. The packaged system should contain all necessary controls and components to meet or exceed NFPA99 recommended guidelines. Systems should be available in simplex and all multiplex arrangements. The factory packaged vacuum system consists of rotary vane vacuum pumps, pre-wired control panel, receiver, and interconnecting wiring and piping, requiring only two plumbing connection. The Medical Vacuum systems should be available as base mounted with vertical receiver size .The vacuum pumps should be continuous duty, rotary vane, oil-sealed, air cooled, direct driven units capable of continuous operation over a working range of 18" to 29" Hg. Each pump should have single shaft seals and should be equipped with an automatic gas ballast valve to prevent condensation of water vapor, extending the life of the oil and the system.
Each pump should be driven by a direct flanged three-phase, standard TEFC motor via a pin and bush coupling. All models should operate between 58-83 dBa,. Pumps require standard automotive grade SAE-30 non-detergent oil for lubrication.
The UL listed I CE marked electrical control panel should be mounted in a control cabinet. The standard
control panel includes the following components:
Integral circuit breaker disconnected with door interlock, across-the-line motor starters with three-phase overload protection
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A programmable logic controller to cycle lead pump with each use
Hand off Automatic selector switch for each pump
Lag pump in use indicator light with horn and connection for remote annunciation
Hour meters to monitor factory recommended service intervals.
Pump running lights to indicate pump in operation.
Each system should include an ASME coded receiver rated for full vacuum service. The system receiver should include a 4-1/2" vacuum gauge, manual drain, and three- valve by pass. Additionally, each system should include properly sized inlet and exhaust flex connectors and vibration isolation pads for filed installation. The pump has the facility that in case one pump stops the standby pump should automatically start. If any pump fails the system should automatically revert to the stand by pump. All the status monitoring of the pump can be connected to the Master Alarm. The system should also include factory installed 5 micron pump inlet filters to promote longer life.
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Standard Bill of Material
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Oil-Lubricated Rotary Vane Vacuum System
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Duplex
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Rotary Vane Pump = 2 Nos,TEFC Motors = 2 Nos,Back Pressure Indicator Gauge = 2 Nos,Oil Reservoir = 2 Nos,Oil Sight-Gauge Glass = 2 Nos,Air Receiver (ASME Rated) = 1 Nos,Three Valve Bypass = 1 Nos,Control Vacuum Switch = 2 Nos,Vacuum Gauge = 1 Nos,Manual Drain = 1 Nos,Electrical Control Panel = 1 Nos,NEMA 12 Enclosure = 1 Nos,Integral Motor Starter with Circuit Breaker Disconnect = 2 Nos,Automatic Alternation = 1 Nos,Running Light = 2 Nos,Hour Meter = 2 Nos,Minimum Run Timer (7.5 hp and larger) = 2 Nos,Control Transformer = 2 Nos,Hand-Off-Automatic Switch = 2 Nos,Lag On Alarm with Horn, Light & contacts = 1 Nos,Interconnecting piping = 1lot Nos,Pump Isolation Valve = 2 Nos,Check Valve = 2 Nos,5 Micron Pump Inlet Filter = 2 Nos,Pump Inlet Flex Connector (installed) = 2 Nos,Pump Discharge Flex Connector (Shipped loose) = 2 Nos,Receiver Flex Connector (Shipped loose) = 1 Nos,Vibration Dampeners (Shipped Loose) = 1set Nos,
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SIIITIC of Vacuum Outlets with matching probes, as per
HTM-2022102-01ofUKINFPA99C of USA as per enclosed technical specifications - (Imported)
Surface mount, non interchangeable, self sealing outlets, outlets should consist of a roughing in assembly and a finishing assembly. A non removable positive- pin keying arrangement for each specific gas service. Installed in the mounting box a fully assembled brass secondary check valve.
Design of outlet should be such that it should have 100% metal construction for corrosion resistance fire safety & push button mechanism for quick release of adaptor. The secondary check valve automatically should form a positive seal to prevent a gas flow when the finishing assembly is removed. The secondary check valve to include 7" (17.78cm) of 1/2" Type K copper tubing with a label affixed which identifies the specific gas by name and colour.
A plastic cap inserted at the end of the inlet tube. Rotation of the inlet tube should allow gas connection from the top or bottom. the finishing assembly should consists of a die cast chrome plated cover plate , a machined brass housing for the primary check valve, and a positive -pin keying device to prevent accidental installation into a roughing in assembly of a dismal gas. The finishing assembly should incorporate a double seal arrangement which automatically engages when a hose adapter or patient treatment device is removed from the outlet. The design of the outlet should be such that if can be easily repaired without disassembly of the outlet.
The finishing assembly should have a colour coded (specific gas) keying disc to prevent connection of hose adapters or patient treatment device to the wrong gas service. The primary check allows absolutely no gas flow to take place until the keying devices are engaged. It should be manufactured in accordance with all applicable NFPA and CGA standards. The locking device should be in the probe instead of gas outlet
Matching probe for outlets- Imported as per NFPA -99 I HTM 02-01 UL Listed ICE Marked Matching probes
to the gas outlet mentioned above. That is adapter for Oxygen & vacuum. Each adapter should have suitable barb or threads so that it can be connected to tube or flow meter /suction regulator. Adapter should have clear gas service embossed on it.
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S/1/T/C of Ward Vacuum unit, as per enclosed technical specifications - (Imported) for critical area The digital vacuum regulator should have a digital vacuum gauge with monochromatic LCD display, it should available with three possible end of scale: -250 mbar , -600 mbar and -1000 mbar.The scale should be able to set in mbar or mmhg by the end user.The numerical display should show the vacuum value and a sector bar proportional to the adjusted de-pressure. The reading resolution is 1 mbar (1 mmhg).The frontal part of the digital gauge should be equipped with 3 buttons: one to switch ON/OFF the vacuum regulator, the other 2 for various settings such as: set the timer for the automatic switch off of the regulator; select the unit scale (mbar or mmHg); set up a preferred vacuum value; zeroing the device at any time.The device should have a quick I/0 switch button that allows the operator to quickly lock and reactivate the vacuum, keeping unchanged the previous preset value. When the device is suctioning, the red button is outside and by pushing it, the operator can stop the vacuum at any time. While, to reactivate the vacuum, at the same pre-set value, the operator should have to simply push the green button (visible when the device is not working).
A vacuum adjustment knob with Soft Grip inserts for an easy handling with a “Push & Lock” position system, the operator should have to pull the knob, by rotating it regulate the level of vacuum needed and then push the know to lock the selected value.Suction jar should be made of polycarbonate and should be auto clavable up to 121ºC. The jar capacity is 1000 ml. The float & cap assembly includes a patient port inlet that is horizontal to help prevent kinking of suction tubing. All collection bottle assemblies should allow visual inspection of fluid level, color & consistency & can be steam autoclaved or gas sterilized
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S/I/T/C of Ward vacuum unit, as per enclosed technical specifications - (Imported) for Other area W.V.Unit should have soft touch knob for easy access to (a) On/off mode (b) Regulation mode (c) full flow of vacuum pressure directly form vacuum line. Mode. The analogue gauge should have 2’’ dia color coded; glow – in – the – dark face for easy readability under any condition. High vacuum setting 0-760" Hg. Suction jar should be made of polycarbonate autoclave up to 121ºC. The jar capacity is 1000 ml. The float & cap assembly includes a patient port inlet that is horizontal to help prevent kinking of suction tubing . All collection bottle assemblies allow visual inspection of fluid level, color & consistency & can be steam autoclaved or gas sterilized. Polycarbonate bottles offer the additional advantage of eliminating breakage.
Filter is designed to help protect the vacuum system from contamination due to aerosols or collection bottle overflow. This high efficiency bacteria filter features a hydrophobic, micro- porous membrane which filters air with maximum efficiency while helping block the flow of aqueous fluids and aerosol contaminants.
Filter efficiency is superb: 99.97% D.O.P. retention (.3 micron particle size). Filters are available with 1/8" NPT male pipe thread on one end to connect to almost any vacuum regulator and a ¼" hose barb for connection of vacuum tubing.
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Supply, Installation, testing & commissioning of Theatre Vacuum Unit (2 jar nos capacity 2000 Ml) (Imported)
Theatre Suction unit shall be a sturdy trolley with base complete with angled high suction controller. The unit shall be powered from the medical vacuum supply and with 5 meter of vacuum hose and matching probe suitable for vacuum outlet. It shall have two suction jars with below mentioned specification.The digital vacuum regulator should have a digital vacuum gauge with monochromatic LCD display, it should available with three possible end of scale: -250 mbar , -600 mbar and -1000 mbar.The scale should be able to set in mbar or mmhg by the end user.The numerical display should show the vacuum value and a sector bar proportional to the adjusted de-pressure. The reading resolution is 1 mbar (1 mmhg)
The frontal part of the digital gauge should be equipped with 3 buttons: one to switch ON/OFF the vacuum regulator, the other 2 for various settings such as: set the timer for the automatic switch off of the regulator; select the unit scale (mbar or mmHg); set up a preferred vacuum value; zeroing the device at any time.The device should have a quick I/0 switch button that allows the operator to quickly lock and reactivate the vacuum, keeping unchanged the previous preset value. When the device is suctioning, the red button is outside and by pushing it, the operator can stop the vacuum at any time. While, to reactivate the vacuum, at the same pre-set value, the operator should have to simply push the green button (visible when the device is not working).A vacuum adjustment knob with Soft Grip inserts for an easy handling with a “Push & Lock” position system, the operator should have to pull the knob, by rotating it regulate the level of vacuum needed and then push the know to lock the selected value.All collection bottle assemblies allow visual inspection of fluid level, color & consistency & can be steam autoclaved or gas sterilized . The jar capacity is 1800 ml 2 nos of bottle . Polycarbonate bottles offer the additional advantage of eliminating breakage.
6
75000
450000
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WAGD/AGSS System
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SIIITIC of WAGD I AGSS system with duplex pump only complete with electrical control panel as per tender specifications as per HTM 2022-02-011 NFPA99C as per enclosed technical specifications
Duplex oil less rotary vane medical vacuum system tank mounted suitable for 03 nos operation theatre on horizontal reservoir provides superior performance with minimal maintenance. The packaged system contains all necessary controls and components to exceed NFPA 99C-2005 STD Latest Edition recommended guidelines.
The WAGD pumps are continuous duty dry-running units with carbon graphite self-lubricating rotary vanes. The pumps are air cooled and direct driven, capable of continuous operating over a working range of 0" to 15 Hg. The pumps are completely self-contained units, requiring no external coolers, pumps, separators or reservoirs. Lubrication is provided by the self-lubricating self-adjusting carbon graphite vanes. The carbon graphite vanes have a life of 8,000 to 15,000 hours, depending on the size of the pump. The pump inlet is protected by means of an integral, 5 micron inlet filter. The rotary design is dynamically balanced and virtually vibration free. The pumps are constructed of heavy-duty aluminum alloy, providing superior heat transfer and long life. The pumps are equipped with large cooling fins and a sound-attenuating enclosure to assure cool, quiet operation.
Remote switches are not allowed for WAGD system as per NFPA-99 Guidelines. The WAGD arrangement has a reservoir hence it provides the WAGD service round the clock. We are providing duplex model of WAGD. If pump in use fails second pump will start automatically without fluctuating in line pressure.
This model operates at 83 DBA. The pumps require no oil or other service liquid for operation.
Each pump is driven by a direct-flanged three-phase standard TEFC motor via a pin and bush coupling.
The UL listed electrical controls are mounted in a NEMA 12 control cabinet. The standard controls include:
Combination circuit breaker disconnects, non reversing, across-the line motor starter with three-phase overload protection
1
1695000
1695000
... More
A programmable controller to cycle lead pump with each use.
Hand-Off Automatic selector switches
Lag pump in use indicator light with horn and connection for remote annunciation
Hour meters to monitor factory recommended service intervals
Running lights indicating pump in operation
The system is supplied with properly sized inlet, discharge flex connectors and vibration isolation pads for field installation. As options, the system can be supplied with a discharge silencer and I or bacterial filters for field installation.
The system includes an ASME coded receiver rated for full vacuum service. The receiver includes a 4-1/2" vacuum gauge, manual drain, and three-valve by pass.
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SIIITIC of WAGD AGSS Outlets with matching probes,
as per HTM-2022102-01ofUKINFPA99C of USA as per enclosed technical specifications - (Imported)
WAGD AGSS Outlet
Surface mount, non interchangeable, self sealing outlets, outlets should consist of a roughing in assembly and a finishing assembly. A non removable positive- pin keying arrangement for each specific gas service. Installed in the mounting box a fully assembled brass secondary check valve.
Design of outlet should be such that it should have 100% metal construction for corrosion resistance fire safety & push button mechanism for quick release of adaptor. The secondary check valve automatically should form a positive seal to prevent a gas flow when the finishing assembly is removed. The secondary check valve to include 7" (17.78cm) of 1/2" Type K copper tubing with a label affixed which identifies the specific gas by name and colour.
A plastic cap inserted at the end of the inlet tube. Rotation of the inlet tube should allow gas connection from the top or bottom. the finishing assembly should consists of a die cast chrome plated cover plate , a machined brass housing for the primary check valve, and a positive -pin keying device to prevent accidental installation into a roughing in assembly of a dismal gas. The finishing assembly should incorporate a double seal arrangement which automatically engages when a hose adapter or patient treatment device is removed from the outlet. The design of the outlet should be such that if can be easily repaired without disassembly of the outlet.
5
7500
37500
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The finishing assembly should have a colour coded (specific gas) keying disc to prevent connection of hose adapters or patient treatment device to the wrong gas service. The primary check allows absolutely no gas flow to take place until the keying devices are engaged. It should be manufactured in accordance with all applicable NFPA and CGA standards. The locking device should be in the probe instead of gas outlet.
Matching probe for outlets- Imported as per NFPA -99 I HTM 02-01 UL Listed ICE Marked Matching probes
to the gas outlet mentioned above. That is adapter for Oxygen & vacuum. Each adapter should have suitable barb or threads so that it can be connected to tube or flow meter /suction regulator. Adapter should have clear gas service embossed on it.
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S/1/T/C of MEDICAL Grade BS EN: 13348 Kite Marked
COPPER PIPE
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-
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12mm
650
795
516750
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15mm
990
1195
1183050
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22mm
1200
1695
2034000
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28mm
250
2245
561250
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42mm
70
2895
202650
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54mm
50
3495
174750
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Copper Piping :
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Installation:
Installation of piping should be carried out as per international standards with utmost cleanliness. Only pipes, fittings and valves which have been degreased as per International standards should be used . Pipe fixing clamps for upto 28mm diameter. Pipes should be non ferrous suitable for the diameter of the pipe. For the pipes of the sized above 28mm rigid metallic hanging or cemented supports to be used.
The main lines to the building to be taken overhead through metallic poles or through underground ducts with inspection removable slabs, All pipe joints should be made using inert gas fluxless brazing method. All joints should be of copper to copper and should be brazed by silver brazing filler material without flux while being brazed joints shall be continuously purged with oil free dry nitrogen to prevent the formation of copper oxide on the inside surface of the joint. All pipes should be installed without springing or forcing. All pipes should be protected against mechanical injury in a manner satisfactory to authorities having jurisdiction.
Test: After erection, all the new pipes cleaned or purged with the help of dry nitrogen gas. Complete system should be tested with dry nitrogen at 2 times of working pressure for 24 hours.
Painting: All existing and proposed exposed pipes/should be painted with two coats of Synthetic enamel paint & color codification as per international standards. All concealed pipes to have gas identification bands I labels at appropriate distance. Similarly all pipes which need embedding in the wall should be tested/painted/labeled and properly insulated.
Certification: To be certified that pipes are suitable for the particular service and complete cross connection
(anti-confusion) test will be carried out.
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Distribution l!il!ing s stem:
MATERIAL {PIPE}:
Solid drawn, seamless, deoxidized, non arsenical, half hard, tempered and degreased materials conforming to BS: EN 13348 Medical Grade Kite Marked Pipe
All copper pipes will be KITE MARKED for medical use before dispatch and the pipe will be delivered plugged or capped at both ends.
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Pipe sizes to be used as under:, 54mmOD X 1.2mm thk, 42mmOD X 1.2mm thk, 28m mOD X l.OOmm thk, 22m mOD X l.OOmm thk, 15m mOD X l.OOmm thk, 12m mOD X l.OOmm thk
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Fittings will be made of copper conforming to BS 864 and suitable for a steam of working pressure of 3S bar and especially made for brazed socket type connections.
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S/1/T/C of MEDICAL AREA LINE PRESSURE (imported) ALARM(Touch Type )- as per HTM 2022/02-01/ NFPA99C as per enclosed technical specifications (imported)
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Area Line pressure Alarm-2 gases
2
175000
350000
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Area Line pressure Alarm-3 gases
4
195000
780000
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Area Line pressure Alarm-4 gases
4
210000
840000
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Area Line pressure Alarm-5gases
4
235000
940000
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Master Main Alarm including all Gases
1
250000
250000
... More
Area Alarms are designed to include all necessary displays, factory wiring, transformers and circuitry requiring only 230 VAC primary powers. Internal voltage should be stepped down to S VDC and 1S VDC for control circuit Power. Voltage to external pressure or vacuum transducers should be 1S VDC.
The Area Alarm should have digital display facility. Each area alarm should monitor up to 6 or 12 medical gas & I or Vacuum services.
Area alarm panels should be modular in design. Each gas monitored should have a light Emitting Diode (LED) display to continuously indicate actual line pressure. A vertical series of LED's should further indicate relative line pressure.
The control module should include a silence/enter button, a Test/Shift button, an Up button and a Down button. These buttons should be used to silence the audible alarm, set up the alarm panel and to test the alarm panel. The test button should test all modules one at a time. An LED on the control module should illuminate green to indicate Power on.
The LED should show Normal pressure at SO psi. Apart from Normal it should also show low risk of 40 PSI as low-pressure and 60 psi as high. High risk of 30 psi as low pressure & 70 psi as High pressure.
Line pressure modules should be available in dual display configuration, dual display modules should accept any combination of pressure or Vacuum.
The back box should contain factory installed copper tube extensions 6" Long, 3/8" ID (1/2"0D) , to accept installer furnished lines form the medical gas system.
Each inlet tube should accept gas - specific DISS fittings for transducers, to prevent cross-connection. The power supply should be installed in the back box Power supply should include an on I off rocker switch and a fuse holder.
The audible alarm tone should pulsate, 90 dBa at 2 meters. The audible signal should be cancelled only by the alarm silence button or fault correction. The display should remain illuminated to indicate the presence of the alarm condition. The alarm should automatically reset with the correction of the fault condition. Should a new alarm occur while the panel is silenced, the audible alarm should reactivate. The area alarm should store the last four alarm conditions in memory at the alarm panel. These conditions can be indicated by using the buttons on the alarm panel control module.
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The alarm should be capable to be connected with the HIS system.
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Line pressure Alarm panel for Medical Gas Piping System should monitor the following indication:-
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2 gas service :
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Oxygen Normal I High I Low Vacuum Normal I Low 3 gas service Oxygen Normal I High I Low Medical Air Normal I High I Low Vacuum Normal I low 4 gas services :- Oxygen Normal I High I Low Nitrous Oxide Normal I High I Low Medical Air Normal I High I Low Vacuum Normal /low 5 gas services :- Oxygen Normal I High I Low Nitrous Oxide Normal I High I Low Medical Air Normal I High I Low Tool Air (Surgical) Normal I High I Low Vacuum Normal /low
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S/1/T/C of MEDICAL AREA VALVE SERVICE UNIT ( VALVE BOX WITH ISOLATION VALVE) AS PER CE CERTIFIED /UL LISTED AS PER ENCLOSED TECHNICAL SPECIFICATIONS- ((imported) )
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-
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2 Gases
2
55000
110000
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3 Gases
4
70000
280000
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4 Gases
4
80000
320000
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5 Gases
4
95000
380000
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ZONE VALVE BOX As per NFPA -99 std I HTM -2022102-01of UK
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Bidder must submitted third party CE certification I UL listed along with tender documents. Self attested
certificate not valid.
( 2 Gas), ( 3 Gas), ( 4 Gas), ( 6 Gas)
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Adopter having opening by quarter turn of handle. The valve should be pneumatically tested as per BSEN 1057 for twice the working pressure and degreased for medical gas service before supply. Valve boxes should be equipped with components for shutting off and supervising individual /parts of central systems in hospital, laboratories and the like. They should be allowed the ward staff to allow isolating of the areas for maintenance and repair work. The pressure monitoring of the distribution system is done by pressure gauges. In case of emergency the door can be glass break opened or by un-locking using the key.
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S/1/T/C of MEDICAL LINE VALVE, AS PER CE CERTIFIED I UL LISTED AS PER TECHNICAL SPECIFICATIONS- ((imported)
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-
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15mm0D
10
6500
65000
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22mm0D
8
8850
70800
... More
28mm0D
4
9950
39800
... More
42mm0D
2
12450
24900
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54mm0D
1
16500
16500
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ISOLATING VALVE, 15mmOD, 22mmOD, 28mmOD, 42mmOD, 54mmOD
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All ball valves as per BS 1057 are rated at 400 psig, as well as full vacuum ( 29.9" Hg). Valves go from full ON to full OFF by turning the vinyl-gripped valve handle 90 ° Locking-type handles may be ordered separately when required. Copper tubing is factory installed to help prevent valve seat damage during soldering. Main and riser valves are not required to be installed in a box unless specially noted or required.
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Supply installation testing and commissioning of Horizontal Bed Head Panel -CE certified as per specifications(indian )
52
34842
1811784
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CE certified
It should provide a safe efficient means of delivering services to patients staff in both general and special care applications, it is modular design made of horizontal aluminium extrusions, and ability to house medical gas termainal units ( as per specifications of tender) and electrical socket , smooth curved surfaces, no visible screws and choice of coloured décor stripe, ease of installation via separate rail-bracket or wall mounting plates, easy removal of covers for maintenance and pipeline connection, with integral twin medical rail as part of the modular extrusion design. It has segregation of services i.e. extra low voltage, normal voltage and medical gases , should be maintained througthout .
Its aluminium extrusions have a polyester coating finish on all external surfaces. It have provision for nurse call, data or monitoring sockets, should be made at the point fo manufacture .It should be supplied duly prepiped , prewired and fully tested or in carcass form. Each Horizontal Bed Head Panel shall be having a provision of (as per outlet distribution list) - four multipin 5-15 Amps , switch socket outlet combine - it should be 1500 mm long.
provision for nurse call
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Total part - I
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Sub: Modular Operation Theater 04 Nos
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S/I/T/C of SMS Walls for 4 nos ofOperating Area as per tender technical specification enclosed european CE certified / UL Listed (imported)
Bidder must submitted third party CE certification along with tender documents. Self attested certificate not valid.
The FRAMEWORK should be made of upright ledgers and profiles entirely made of a galvanized steel sheet with a thickness of 1.5mm. They should folded structural steels with a suitable section for the loads. The structure components should be joined together by means of coupling systems in order to create a solid reticular frame, able to support different infillpanels whose weight is up to 8 Kgƒsqmtr the "Z" upright forms the vertical part of the frame and should be equipped with proper drilling of 32mm ( height partial drilling) suitable for the panel coupling without suing screws between the prights and edges of the panel there is a suitable PVC adhesive seal with a thickness firm of 3mm to ensure air and dust sealing. At the lower end of the upright an adjustment foot should allow the easy leveling of the structureand, the necessary compression of the anchorage between ceiling and floor.
The ledgers should the elements that constitute the basic module of the structure. They should be inserted on the proper hooks by pressure between two uprights, Moreover some "U" profiles , to be placed in horizontal position on the upper and lower part of this structure, constitute its extension with a depth of 64mm together with the metal panels with a thickness of 18mm and the PVC adhesive seal. The structure can be provided with stiffening ledgers or profiles for sliding door fixing and other accessories according to needs. Total thickness of the partitionwall:100mm
Skin PANELS ( double wall 1 side−partition wall 2 sides):
Module skin panels should have a height exceeding 3 mtrs up to a maximum of 3.5m from the floor and a width that should vary from a minimum of 280mm to a maximum of 1200mm"they can be made of different types of finishing; using solid surfacematerial
300
46500
13950000
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The panels should be made of solid surface material thick 3mm backed by structural panel thick 15mm consisting of a trapezoidal aluminium corrugated core glued between two flat of aluminium sheet. The Solid Mineral Surface (SMS) material should be dent free antibacterial & fire resistant. The Solid Mineral Surface (SMS) should not require any paint & should have in built antibacterial properties. The material should be manufactured for about two third with aluminiumhydroxide and a third with acrylic resin and natural pigments. The aluminium hydroxide should give the product a particular strength and the quality of the acrylic resin should ensure cleanliness, water resistance and colour stability over time. The material should have antibacterial activity (% reduction99%).
On the inner sides of the panels there should slotted holes for their anchorage to the support
hooks fixed to the structure uprights, This fastening system should allows obtaining all the following results:
The panel should be self centering with consequent joint alignments between panel and panel, ensuring aesthetic balance.
The connection between hook and panel should be designed so that the panel, due to its weight, is compressed against the PVC seals coating the entire structure helping to reduce noise transmission. The fixing system of the panels should ensures that there is no accidental breakaway of the panel, even If it is subjected to stress for more safety andstability:
The connection system should allow disassembling and assembling each panel without moving the others near it. Its flexibility the partition wall should satisfy all the inspection and ƒor the maintenance needs required by modern workplaces (for example electrical installations, hydraulic installations, medical gases etc.) all the panels can be removed over their entire length and on both sides. The lower part of the panel should be equipped with a profile prepared for the laying and the coupling of the horizontal skirtings that need to re enter with the respect to the panel.
The inner angles (which are at 90 degree) in operating rooms or in similar environments should made up of a panel without interruption of continuity that covers the angular area of the wall. The panel should characterized by a double specular folding at 135 degree ( or variable folding according to the requirements). All the panels should be drilled according to specific needs ( ex ventilation grids of the room) The panels should be perfectly sealed together by means of thermoplastic rubber gaskets inserted by pressure and free of projections.
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Properties & Features of Solid Mineral Surface Material ., Density g/cm3 1,7, Hardness (Barcol) 60, Water Absorption % 0,023, Heat Expansion (1 x 10”in/in”/F) 2,1, Ignition Test 38, Tensil Strength, psi 6500, Elongation At Yeld % 0,2, Flexural Strength, 8ft;o,5lb 72D-79000, Water Resistance, g/1000cycl Unbreakable, Lustre Stable Resistance 0,05, High Temperature Resistance Uninfluential, Boiling Water Resistance Uninfluential, Stain Resistance Uninfluential, Chemical Resistance Uninfluential
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S/I/T/C of Ceilling for 4 nos of Operating room as per tender technical specification enclosed european CE certified / UL Listed (Imported)
100
35500
3550000
... More
Bidder must submit third party CE certification along with tender documents . Self attested certification not valid.
The hermetic suspended ceiling should be a loading structure in heavy gauge material forming the frid on which the ceiling panels (made of steel painted material Imported). The modular grid, which can be 600 x 600 mm, or variable, allows the integration of sealed lighting fixtures, air anemostats and / or various service units. The variable module grid should make it possible to adapt the size of the ceiling module to match the equipment to be mounted. It should also allow the use of different module sizes within the same room.
The grid should be formed of loading profiles, suspended from the ceiling slab, to which the crossbar profiles are secured by means of rigid mechanical couplings. The thus formed grid should be rigid and remains perfectly stable during all the subsequent site operations.
The suspended ceiling should be hermetically sealed by means of silicon gasket application. The function of silicon sealing should be that of assuring an airtight environment in the room and eliminating cervices in which dust could accumulate. The gaskets to be made of non toxic silicon in compliance with regulations applicable to clean rooms .
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S/1/T/C of Laminar Flow (Planar Ceiling of size 2400mm X 2400 mm ) constructed out of 1.6mm thick aluminum sheet complete set, as per enclosed tender technical specifications duly CE Marked (Indian)
The plenum box (2400mm x 2400mm) will be made of high quality Aluminium 1.6mm thick & Air diffuser will be made of Woven polyester cloth that will introduce the highest air quality into the Operation Theatre. There will be 8 HEPA filters (as per plenum size) with 99.97% efficiency to ensure high quality clean air & tight control of bacteria infection system. Air will be diffused into the theatre uniformly over the total area through perforated aluminium sheet. The air distribution system serving to the Operation Theatre will be tested as per DIN 4799 standards.
The laminar flow installation & lighting system will be design to provide the Operation Theatre as key to preventing patients being infected during operation lies on the design of sterilized air conditioning system and the flow pattern of draught as well as the quality of engineering.
The ceiling will incorporate supports to secure it to the main structural frame of the modular operating theatre.
4
445000
1780000
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SITC of recess mounted cleanroom flat LED panel of 595 x 595 mm size fully lit diffuser (cct 6500K) suitable for clean room applications with efficacy better than 100 Lumen/watt (minimum total lumen delivered package 5000 ), with CRI 80,THD5% & Driver efficiency 90% .Service life of 50,000 hrs @ L 70 etc complete as required. (Approved Makes :(Zumtobel/ Philips/ TRILUX/ENDO/LT)
Six sets of double peripheral OT lights each set having two lights will be provided with stepped finish aluminium reflector and will be of A class for use in clean room application. The peripheral light diffusers will be constructed from opal prismatic diffuser material in aluminium frames.
Light will be generated from high frequency electronic ballast's complete with colour corrected fluorescent tubes. The ceiling will incorporate supports to secure it to the main structural frame of the modular operating theatre. The laminar flow ceiling will be able to provide integrated lamp support system, ease of maintenance and long life system. Control equipment for the peripheral lighting will be provided in the theatre control panel to allow independent control of the lighting levels by the surgical team.
The operation procedures can never be affected by shadows, shimmering lights and dazzling eyes. This has been achieved by the lighting system with sufficient illumination level at the wound site and to provide flicker less design lighting control system
Controls for the peripheral lighting will be provided in the theatre control panel to allow independent control of the lighting levels by the surgical team.
32
9950
318400
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S/1/T/C of Touch type Surgeon control panel, mounted flush in the theatre wall, complete set with electrical Distribution Board, as per enclosed tender technical specifications. (Imported)
4
995000
3980000
... More
The Control panel will be Touch Screen size not less than 19" Medical Grade , can be configured to incorporate all the services that Operation Theatre staff required. The connection between the surgeon control panel and the distribution board will be by a multiplexed system, providing a PWM signal on a two− corecable.
The panel will contain 6 services Tiles as follows:]
a). Time day clock
b). Time Elapsed Clock
c). Temperature & Humidity Indicator
d). General/peripheral Lighting control
e). Medical Gas Alarm Panel- upto 6 gases
f). ). Hand Free telephone.
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Time Day Clock will be digital type and clocks have high brightness characters, not less than 30mm in height. Time Elapsed Day Clock will be digital type and clocks have high brightness characters, not less than 30mm in height. Temperature Indicator will indicate the theatre temperature will be connected to the local pressure switches of Air-Conditioning system. Indicator will be digital type have high brightness characters, not less than 30mm in height.
General Lighting System incorporates all the necessary controls of the lighting system inside the theatre. The medical gas alarm will indicate High and Low gas pressure for each gas service present in the operating theatre and will have an audible buzzer with mute facility. The medical gas alarms will be connected to local pressure switches located downstream of the last isolation valves.
The size of the each tile will not be more than 300mm x 200mm. Colour will be RAL 9002 for the frame and membrane fascia. The Control Panel will be designed for front – access only.
All high voltage equipment is installed in a separate enclosure. The remote cabinet will house the operating lamp transformers, mains failure relays, electrical distribution equipment and circuit protection equipment for all circuits within the operating theatre. All internal wiring will terminate in connectors with screw and clamp spring connections of the Clip−on type mounted, on a DIN rail and labeled with indelible proprietary labels. Individual fuses or miniature circuit breakers will protect all internal circuits. All internal wires will be marked with plastic ferrule type cable markers,
for ease of identification.
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S/1/T/C of Twin Plate X-ray viewing Screen designed to provide a high level of control luminance without flicker. Size:- 1000x700x95 Deep, indigenous, complete set as per enclosed tender technical specifications. (Indian)
The theatre will be equipped with a 2-plate X-Ray viewing screen. It will be designed to provide flicker free luminance for the film viewing purpose. It is installed flushed with the theatre wall for hygienic and ease of cleaning purpose. The X-Ray viewing screen is designed for the purpose of front access. The X-Ray viewing screen will be illuminated by 4 pieces of high frequency fluorescent lamps and the dimming will controlled by the usage of dimming ballast with Philips make rotary control. The diffuser is able to diffuse the light evenly and to provide enough luminance for film viewing. It is made of high quality opaque acrylic sheet. The film is held firmly by using spring-loaded clips for ease of mounting and demounting. The body is built by using electrolyzed steel with powder coated to BS standards.
4
35000
140000
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S/1/T/C of Seamless flooring with perfectly curved fish-covings resistance to mechanical stress and dynamic load and having Electro static discharge (ESD) I (anticonductive) protection characteristics 3mm thick, washable- complete. As per enclosed tender technical specifications. (Imported)
The floor finish in the operating room will be 2-3mm Static dissipative PVC tiles, laid on a semi conductive adhesive base. The floor finish will terminate at the room perimeter passing over a concealed cove former and continuing up the wall for 100mm.
Flooring will fulfill EN 649 of US requirements. It will have chemical resistance as per EN 423 . It will have electrical resistance conforming to EN 1081/IEC 61340.
All joints will be welded and the plastic wall finish will overlap the floor caving by 25mm, to provide a continuous sealed surface.
A floor screed will be provided, flat to within a tolerance of+/- 3mm over any 3-metre area. Onto this sub floor, a self-leveling compound will be laid prior to laying of the floor finish.
The self-leveling compound will be of the type that does not promote bacteriological growth. Copper grounding strips (O.OSmm thick, SOmm width) will b laid flat on the floor in the conductive adhesive and connect to copper wire of grounding
160
4950
792000
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S/1/T/C of Scrub Sink- 2 bay- made in Stainless steel 304 Finish, having Sensor & Foot Operated with Thermostatic Mixing valve control to Size maintain the water temperature, Indigenous complete set, as per enclosed tender technical specifications.(lndian)
The scrub station will be equipped with 2 bay scrub stations. The scrub station will be made of high-grade stainless steel 304 with stain polish finish and wired to the current lEE regulations & BS 7971. The scrub stations control system will be based on advanced microprocessor. The scrub station will be sensor-activated 24VAC. The scrub station will be provided with user selectable time out control. The supply will not be interrupted in case of power failure or maintenance.
The station will be equipped with thermostatic mixing valve to control the temperature of hot I cold water supply. The washing faucet will be made of Chrome plated brass hand.
2
145000
290000
... More
S/1/T/C of Automatic Sliding door, Complete with Automation Unit, frame, viewing window. complete set, as per enclosed tender technical specifications. (extruded aluminium) (Indian)
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-
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Each 2100mm x 1500 mm (height x width of door frame)Automatic
4
595000
2380000
... More
S/1/T/C of 1OOOmm x 1000 mm vertical blend Motorized window (Indian)
1
115000
115000
... More
This should be a hermetically sealed, single sliding door (Standard Size: 2.1 m x 1.5m/2.1xl.O m)
The controller should be capable of being operated by elbow switches/foot switches as well as touch less
sensor.
The track should be of stainless steel/Aluminum and the running surface for the top rollers should be suitably angled to reduce resistance to movement
The door leaf should be hung by means of hard plastic rollers of high quality with double bearing at the top. Rollers should be provided under the stainless steel/Aluminium track to enable smooth and noiseless movement.
Opening and closing of the door should be microprocessor controlled electromechanical movement.
The door material should be of HPL Color should match the interior and care should be taken to make the leaf strong and light weight.
One should be able to open and close the door effortlessly incase of failure of automatic mechanism.
Door opening handle should be strong and sturdy. Material should be of 55 (gloss finish). Should be provided with high quality cylindrical lock.
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Door leaf should have high quality synthetic rubber gasket with long life to ensure hermetic sealing (to maintain air pressure differential). Air tightness 99.99% at a pressure of lOOPa.
The finished floor on either side of the door should be perfectly level (maximum permissible difference +lmm).
The overall thickness of the finished door should be 55 to 60mm. The inner part of the door should be filled with CFC free polyurethane foam thickness of 48mm or nearby. (Sealed airtight to prevent further ingress of any microbial organism).
The door and controls should comply with lEE regulation. All motors used should be DC brushless motors with essential isolation from mains.
Door should be with vision window 300 mm x 300 mm with double glazed panels and hermetically sealed.
Door movement should have minimum noise.
The starting time after receiving the signal should be adjustable between 0.5 to 20 seconds.
The door controller should be CE marked.
Test certificate for hermetically sealed door frame (factory test certificate) should be enclosed with the pre dispatch documents.
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S/1/T/C of LED OT light European CE Certified/UL listed IFDA as per technical specifications.(imported)
should have the following Features: Two Major Dome/light head,Single Colour Pure White LED,s,Reflector based LED Technology,Arrangement of LED in such a way that Shadow Free / Deep cavity illimination is achieved,Special design to maximize the field of illumination and optimized illumination depth,should have good laminar flow properties,Easy and less time consumng service access of electronics on the light head dome surface, Aluminium Housing for better heat management, ESG safety glass for simple and fast disinfection process,360 deg rotation of domes/lightheads / arms for unlimited positioning of light heads,MIS Lightning Feature on domes, Technical Data of Light Heads: Major (2) ,Central Illumnination Ec (1mt) 160,000 lux,Intensity Range (Lux) 30%-100%, Life time of light source (h) /= 50,000,Light Field Diameter (mm) 180-300,Depth of Field L1+L2 (mm) /= 850,CRI (Ra) /=96,R9 /=96, Colour Temp(K) /=4500,Rated Power Output less or equal to 65W at 24V DC,Light Head Power Consumption 200 VA+/- 10%, Radiant Energy around 3,4mW/m2lx,Temp increase 1 deg,Power Supply-Primary Voltage(V AC) 90-240,Rotation 360 deg,Operating Range /= 1700 mm,Adjustment of the spring arm / = 1175 mm,Approx wt of each LH /= 18kg
4
1995000
7980000
... More
S/1/T/C of camera for OT light as per technical specifications.(imported)
Specifications for Centrally Mounted Camera System
Should have the following Features:To be mounted on central area of LH should have a wall mounted control,Technical Data: Sensor : 1/4" Super HAD CCD,Lines and Gaps: 768x576,Video standards: PAL,Pixels: minimum 444000,Aspect Ratio: 4-3,16-9,Minimum Illumination: 1 Lux,S/N Ratio 50 dB,Minimum working,distance: 10mm/Wide,800mm/Tele,Power Supply : via LH/ Max 12 W,Video outputs: Y/C,IT port: RS 232,Zoom 18x optical zoom,4x digital zoom,f:4.1-73.8 mm,Power Supply: via OR light, max.12 W,Image stabilizer Yes,Focus Automatic, manual,Iris: Automatic, manual,White balance: Automatic, manual
1
595000
595000
... More
S/1/T/C of Flat panel monitor as per technical specifications.(imported)
Should be 30-32” High Definition Progressive Scan Flat-panel Medical Grade Monitors with ceiling,The flat Panel suspension should be ready with the cables for integration of High Definition Digital (DVI/HDTV), RGBHV (High Resolution), SVHS (S-Video), Composite video signals to travel from the various sources of video like endoscopic camera, room camera, in light camera, high definition flat panel monitors, while assuring native resolution / signal.
1
495000
495000
... More
S/1/T/C of Single Arm Pendant with 1OOOmm long horizontal arm with both horizontal and vertical movement , imported, as per CE Certified / UL Listed, complete set, as per enclosed tender technical specifications. (Imported)
Bidder must submitted third party CE certification along with tender documents. Self attested certificate not valid.
Multimovement Pendent is a new design motorized Single arm(900mm)with up & down movement of 515 mm and load carrying capacity of 150 kg. The arm can be rotated upto 330Q- 340Qwith adjustable stopper. An extremely quite electric motor reduces noise to a minimum, dampened stoppers and very low hand forces for horizontal movements contribute to an ergonomically optimized workplace. The newly developed pneumatic brake system can be adapted to various safety requirements and construction facilities. Modern and very quiet, high performance motors as well special spindles are used to realize precise & steady movement. As a safety feature the motor is equipped with an over load protection. The large interior cross section for supply lines offers completely new applications with 120 mm diameter. The stoppers are infinitely variable from 0-330Q-340Q
4
1395000
5580000
... More
Service head is provided with the modular design square in shape to achieve maximum supply with minimum required space. Service head is designed to hosts, Base, Gas Module, Electric Module and shelves. Upto 8 Gas outlets & 10 Electrical switches. Racks & shelves are provided to mount the equipments like monitor etc. The total length of the manager is 800mm. Anesthesia pendent will have one arms with shelves as per following details:
a. Horizontal arm system - 1
b. Weight carrying capacity - 150kg
c. 5/15 Amp. Electrical sockets without switches - 10 Nos.
d. Shelves with side rails - 2 Nos.
e. Provision to fix Gas outlets(i.e.) Oxygen- 2, Vacuum- 2, Air 4 bar-1, Air 7 bar-1, N20 -1& WAGD-1no.
f. Gas interface set for interface plate - 1
g. Ceiling mounting system for interin ceiling upto 1000 mm - 1
h. Interface plate with electrical fittings - 1
i. Ceiling cover for interin ceiling - 1
J 2 nos LAN points with RJ 45
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-
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S/1/T/C of Double Arm pendant with 1000mm+800mm long horizontal arms with both horizontal and vertical movement , imported, as per CE Certified/ UL listed, complete set as per enclosed tender technical specifications. (Imported)
Bidder must submitted third party CE certification along with tender documents. Self attested certificate not valid.
Multimovement Pendent is a new design motorized (1000+800) arm with up & down movement of 515 mm and load carrying capacity of 150 kg. The arm can be rotated upto 330Q- 340Qwith adjustable stopper. An extremely quite electric motor reduces noise to a minimum, dampened stoppers and very low hand forces for horizontal movements contribute to an ergonomically optimized workplace. The newly developed pneumatic brake system can be adapted to various safety requirements and construction facilities. Modern and very quiet, high performance motors as well special spindles are used to realize precise & steady movement. As a safety feature the motor is equipped with an over load protection. The large interior cross section for supply lines offers completely new applications with 120 mm diameter. The stoppers are infinitely variable from 0-330Q-340Q
4
1495000
5980000
... More
Service head is provided with the modular design square in shape to achieve maximum supply with minimum required space. Service head is designed to hosts, Base, Gas Module, Electric Module and shelves. Upto 8 Gas outlets & 10 Electrical switches. Racks & shelves are provided to mount the equipments like monitor etc. The total length of the manager is 800 mm. Surgeon pendent will have 2 arms with shelves as per following details:
a. Horizontal arm system - 2
b. Weight carrying capacity - 150kg
c. 5/15 Amp. Electrical sockets without switches -10Nos.
d. Shelves with side rails - 2 Nos.
e. Provision to fix Gas outlets(i.e.) Oxygen- 2, Vacuum- 2, Air 4 bar-1, Air 7 bar-1, WAGD-1no.
f. Gas interface set for interface plate - 1
g. Ceiling mounting system for interin ceiling upto 1000mm - 1
h. Interface plate with electrical fittings - 1
i. Ceiling cover for interin ceiling - 1
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S/1/T/C of writing board, indigenous, complete set as per enclosed tender technical specifications. (Indian)
One Operating List Board should be provided in each Operating Theatre and should be made of Ceramic Magnetic white board. Operating List Board should be flush mounted.
4
18500
74000
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S/1/T/C of PRD , indigenous, complete set as per enclosed tender technical specifications. (Indian)
Pressure Relief Dampers should be provided in each room to prevent cross contamination of air from clean and dirty areas. Suitably sized air pressure relief damper should be strategically placed, enabling differential room pressure to be maintained and ensure that when doors are opened between clean and dirty area. Counter-weight balancing system should be provided in the PRD to maintain positive pressure inside the operation room. Air pressure stabilizers should have unique capability of controlling differential pressure to close tolerance. The PRD should remain closed at pressure below the set pressure and should open fully at pressure only fractionally above the threshold pressure.
The body should be epoxy powder coated as per standard BS colors. First class electrolyzed steel plate should be used for body and with high grade SS304 Stainless Steel for bladders.
4
52000
208000
... More
S/1/T/C of Storage Unit , indigenous, complete set as per enclosed tender technical specifications. (Indian)
The storage unit should be made with 1.50 mm thick SS sheet panels. Storage Cabinet should be divided in two equal parts and each part should have individual glass doors with high quality locking system. Each part should be provided with racks.
4
65000
260000
... More
S/1/T/C of DUCTING inside OT as per enclosed tender technical specifications.
The internal ducting inside of the Operattion theatre should be done duly fabricated out of 22 /24 swg Aluminum sheet complete with flanges and accessories such as GI suspenders and GI supports completely sealed with Silicon sealant duly insulated with Aluminum foil Nitrile rubber self adhesive type insulation. e. ELECTRICALS Wall / Floor mounted control panel comprising of contactors / starters Nos. 1 for Heaters, AHU Fan motor, switch fuse unit for Condensing unit, complete with indication lights etc. Supply of Power cabling, control wiring & GI earthing assuming that Lot 1 Electrical panel should be located at a maximum radial distance of 10 Meters from AHU / Condensing unit. [Main power supply terminating at each Condensing unit and our Control Panel to be provided by Client ]
4
245000
980000
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S/1/T/C of Electrical wiring inside OT as per enclosed tender technical specifications. Modem medical procedures utilize and increasingly rely on, electrical and electronic equipment. This equipment ranges from lighting to patient monitors and electrosurgical equipment.
Power distribution within "the departments should be "provided' from distribution boards located local to each theatre. Sub mains power to these panels should be by the general electrical contractor. From these panels all distribution services within the departments should be run.
Power sockets within the Operating Theatres ancillary areas .
All equipment should be fully and permanently labelled to identify and describe the function, operation and voltage of the apparatus concerned. Throughout and upon completion of the electrical installation, tests in accordance with relevant sections of the local wiring regulations should be carried out and the results recorded
4
125000
500000
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OT integeration as per specifications for 1 OT (imported)
SECTION 1- HD LED Medical Monitor with monitor arm
Specifications:
a. 26" HD LED Medical Grade Monitor
Specifications:
Patient Video and image Management System in OT
The system should be FDAƒCE approved and be able to integrate all Video signals available inside OT. It should have digital surgical time out verification check list. It should be able to manage the following Inputs andOutputs.
S. No. Input(Source) Signal-Type Output (Destination)
1. Endoscopic Cameraƒ DVI Monitor 1 onSpring
Operating Microscope arm of the OT light DVR
2.In−Light Camera DVIƒHD−SDI, Monitor 2 on the S− Video arm of the Surgicalcomponent Pendant, DVR
3. PTZ RoomCamera S−Videocomponent DVR
4. C−ArmƒNavigation S−VideoƒVGAƒDVI Monitor 3 System
5.Patient Vital Sign VGA, BOOL DVR ArchivingSystem
6.ArchivingSystem S−Video component, DVIƒHD−SDI
7. Free for Future Use
8. Free for Future Use
The system should have 10" or more TableƒTouch Screen based control. The same should allow the surgeon to see more than 1 image on any of the monitors in PIP and PAP mode as well as move the position of the images as per hisconvenience.
The system should have provision to record the video sequences from OT and overlay the surgical time and vital signs on all video streams emanating from the OT and also user selectable streams for live viewing outside the OT or for videoconferencing.
1
8895000
8895000
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The full High Definition Dual channel Digital Documentation System for parallel recording of videosƒstills from two video sources should be a high−end computer system bases on Windows 7 embedded platform with inbuilt access security, designed spec—for recording, managing and archiving surgical images and video in native full HD resolution. The inbuilt storage capacity shall be for a minimum of 100 hours of all video feeds or at least 1TB whichever’s more.
It should have integrated surgical checklist following the WHO standard
The captured full high−definition images & videos shall be accessible from the hard drive for printing or saving onto multiple forms of external media which includes CDƒDVD, USB Flash Drive & Hospital network via separate 12" or more touchscreen.
It should allow for storage on internal memory (2TB FIRO), USB storage media via 2.0 and 3.0 optical media, network drive, FTP.
It should allow for intelligent, adaptive storage management and Automatic storage in the background to reduce the time between the surgical procedures.
It should have integrated security software as a protection against malware, independent from security patches of the operating system and it is only possible to run certified software.
It should have internal memory SSD (70GB or more), HDD (2 TB or more), Memory RAM 8GB or more.
It should allow for
Image format BMP,JPG, JPG2000
Video format MPEG−4, MPEG−2 MOV
Video signal inputs 2x DVI−D
Color system: PAL, NTSC
Resolution still images up to 1920x1080, Aspect ratio 16.9
Resolution videos up to 1920x1080 Progressive Scan for 25ƒ30 frames.
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Total part - II
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-
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Sub: CSSD
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HIGH SPEED FULLY AUTOMATIC STEAM STERILIZER Capacity and Dimensions a. Minimum Volume:400 to 450 Liters
b. Shape: Horizontal Rectangular. Design and Construction a. Vertical Sliding Doors with automatic locking.(Pneumatic/Motorized b. Temperature range 105 °C (221 °F) to 138 °C (280 °F). c. 48 kW or more electrical steam generator d. Pressure gauges on front panel (chamber and steam generator). as per specifications
e. Pressure gauges on front panel (chamber and steam generator). f. 316L stainless steel chamber. jacket & stainless steel door g. Electro polished chamber in addition to a mirror-like finish (0.6 to 0.8 micron). h. 0.2 micron Hepa filter for air to enter the chamber during vacuum break. i. Provided with wheels, for convenient autoclave loading carriages and trolley. j. Chamber Steel 316L Jacket 316L and doors 316L. Machine should be registered with CDSCO under provisions Medical Device Rules 2017.
1
5500000
5500000
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FULLY AUTOMATIC STEAM STERILIZER CSSD Steam Autoclave should be able to be able to sterilize wrapped instruments, unwrapped instruments, linen, glassware and liquids.
b)The autoclave should designed to operate on various pre select programs such as fabric, Instrument cycle, Liquid Cycle ,Gravity ,Prion and two standard Bowie Dick & Helix Test and Vacuum Leak Cycle c)It should be provided with a single manual door with all fully automatic operation of the entire cycle once the door is closed manually.
d)Sterilizer should meet all international standards such as A.S.M.E/PED for Pressure vessel, and e)Should be European CE certified by third party having 4 digit marking in accordance with Medical Device Directives (MDD) 93/42/EEC, as per specifications. Machine should be registered with CDSCO under provisions Medical Device Rules 2017.
1
2950000
2950000
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WASHER DISINFECTOR WITH INBUILT DRYER, DOUBLE DOOR Dimension: Chamber: Width 560mm Depth: 585 mm Height: 780 mm or Higher
2. Chamber Volume: 265 Liters or higher
3. Door Type manual Hinged type/ Automatic Sliding door
4. Loading Capacity 10 Din Baskets in 5 layers or more.
5. LCD (70x50) graphic display located on both sides A powerful Washing Pump for washing and drain with 0.8Kw rating. The washer should be USFDA/ European CE and latest ISO certifications as per specifications . Machine should be registered with CDSCO under provisions Medical Device Rules 2017.
1
3900000
3900000
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Drying Cabinet 350 liters or more as per specifications
1
319308
319308
... More
ULTRASONIC CLEANER 28-30 liters (1 No.) 1. Should be made of Stainless Steel SS 304 quality, 18 SWG thickness of body, door and panelling. 2. Shall be designed for ultrasonic generation with PZT transducers for mechanical vibration in the cleaning liquid 3. Shall have a minimum volume of 28-30 liters, with ultrasonic frequency of 30 KHz (+/- 3 KHz), ultrasonic power of 500 Watts 4. Should be supplied with suitable SS Lid and baskets as per specifications
1
545160
545160
... More
Table Top Sterilizer 22-24 liters capacity Class B type as per specifications Machine should be registered with CDSCO under provisions Medical Device Rules 2017.
2
356950
713900
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STAINLESS STEEL WORK TABLE WITH DOUBLE SINK 1.Complete stainless steel SS 304 body construction, 18SWG thickness. 2. Shall have provision for attaching spray gun rinser (air / water) 3. Separate hot and cold water faucet above each sink 4. Shall have Two Sinks made of stainless steel SS 304 quality, 16SWG thickness, are designed in a way to minimize splash . Machine should be registered with CDSCO under provisions Medical Device Rules 2017.
1
250000
250000
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SPRAY GUN RINSER WITH EIGHT ATTACHMENTS Various sizes and shapes of minimum eight attachments made of good quality Stainless Steel to be used for cleaning syringes, catheters, endoscopes, cyst scopes, other instruments and articles used in sterile services. 2. Shall be capable for minute jet of spray of water / compressed air 3. 1/4"BSP connection with SS breaded Hose for water & air 4. The water and air pressure should be released, regulated and fully controlled by the spray gun trigger. 5. Should be suitable to be connected with the wash station with double tank. as per specifications. Machine should be registered with CDSCO under provisions Medical Device Rules 2017.
1
55000
55000
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SS CONTROL & PACKING TABLE WITH DRAWER 1.Shall be made of good quality Stainless Steel SS 304, thickness of 18 SWG 2. Shall have minimum two shelves for separation, control and packing of various sets of sterilized goods forwards, clinics, operation theatre etc., 3. Shall have Stainless steel 304 quality drawers, 18SWG thickness, underneath the table and also with nylon adjustable leveling bullets for legs 4. Shall be provided with minimum one drawer in the table 5. Shall have provision for electrical connections for sockets of 5 Amps & 15 Amps as per specifications. Machine should be registered with CDSCO under provisions Medical Device Rules 2017.
2
140000
280000
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STAINLESS STEEL WORK TABLE WITH UNDER SHELF 1. The table top fabricated out of 16 SWG SS 304 grade, ground and polished to a smooth surface without high edge sections. 2. The table top frame a complete assembly with front, back and two ends welded together at corners. 3. Suitable undershelf to be provided as per specifications. Machine should be registered with CDSCO under provisions Medical Device Rules 2017.
3
168740
506220
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TABLE MOUNTED HEAT SEALING MACHINE 1. This sealer with conveyor is suitable for small bags packaging and adopts electronic constant temperature control system and speed adjusting transmission mechanism. It can seal plastic films of various materials. 2. Temperature Range: 0 – 300oC 3. Sealing speed: 0-12mtr/min 4. Sealing film thickness: 0.02-0.80 mm 5. Sealing width: 6-15 mm 6. Power consumption 500 W as per specifications . Machine should be registered with CDSCO under provisions Medical Device Rules 2017.
1
260000
260000
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SS BASKET RACK • SIZE(LXWXH) : 1850* 480*2150MM(Single), 1850*800*2150mm(Double) • Single and double basket storage racks to store wire baskets in sterile storage • The rack should be designed as an open unit to have aeration of sterilized goods and to make inspection of stored goods easy and convenient. • Should have rigid, horizontal guide rails, consisting of 50*20 mm steel profiles for loading and unloading the baskets by sliding the baskets on rail. as per specifications. Machine should be registered with CDSCO under provisions Medical Device Rules 2017.
2
110330
220660
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SS PASS BOX DOUBLE DOOR 1. The Pass Box shall be fabricated from S.S. 304 stainless steel sheets with double wall construction. 2. Should have full argon welding for superior hygiene 3.Shall have UV lights for safe storage of components. 4. Magnetic locks for both doors must be there. 5. Door interlocking to prevent simultaneous opening of both doors. as per specifications . Machine should be registered with CDSCO under provisions Medical Device Rules 2017.
3
181720
545160
... More
STAINLESS STEEL STORAGE RACK WITH FIVE SHELVES 1. Shall be made of good quality Stainless Steel SS 304; Size: 1830mm L x 535mm W x 1830mm H 2. Floor mounted type, storage rack with five shelves to store the medical instruments / linen 3. Frame shall be fabricated of 40mm square Stainless steel pipes, legs shall be provided with adjustable nylon Bullet feet; Frame thickness , 14SWG. as per specifications. Machine should be registered with CDSCO under provisions Medical Device Rules 2017.
6
97350
584100
... More
BASKET FULL SIZE • Size: 585X395X195 mm • It should be modular design with standard spri sizes and high precision and should be design for sterilizing/processing as well as easy handling and management of the supply, storage and distribution of re- circulated sterilized goods. as per specifications Machine should be registered with CDSCO under provisions Medical Device Rules 2017.
24
8437
202488
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BASKET HALF SIZE • Size: 585X395X100 mm
• It should be modular design with standard spri sizes and high precision and should be design for sterilizing/processing as well as easy handling and management of the supply, storage and distribution of re- circulated sterilized goods. as per specifications
Machine should be registered with CDSCO under provisions Medical Device Rules 2017.
24
7139
171336
... More
CLOSED TRANSPORT TROLLEY • Size: 1400X750x1260 mm ( L*W*H) external. • Closed transport trolley is needed for sterile goods handling with requires higher protection than normal dust protection. Should be suitable to handle baskets or containers with total capacity of 6 STU or three solid removable shelves. • Trolley should have large S.S wheels for easy maneuverability. • Should have two fixed and two swivel wheels with brakes. as per specifications Machine should be registered with CDSCO under provisions Medical Device Rules 2017.
4
162250
649000
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