Retender for Supply, Installation and Commissioning of BicarbonateMixer, Fumigation Dispensor, Suction apparatus and Syringe Pump for 8 bedded Dialysis unit at PHC Ajanur

Amount

Bicarbonate Mixer

1. Should have conical bottom type vessel of capacity atleast 100litres, made of Lipde (linear low-density polyethylene) material. Supporting stand should be made of Stainless steel – SS 304 grade. 2. Should have stainless steel rod grit, non wetted pedestal stirrer - Not applicable in case of pressure flow mixing technology. 3. Should have Marine style 3 blade propeller- Not applicable in case of pressure flow mixing technology. 4. Blade should be stainless steel – SS 316 L grade or Pressure flow mixing technology. 5. Should have at least 0.5 Hp, single phase electric motor, 230V AC. 50 Hz. 6. Motor Assembly shall be quickly removable for easy cleaning and autoclaving. 7. RO water inlet should be Cpvc with ball valve @ 105 ltrs. 8. RO water outlet should be Cpvc with ball valve @ 100 ltrs. 9. Solute should be Cpvc with ball valve @ 4 ltrs. 10. Drain should be Cpvc with ball valve @ 0 ltrs. 11. Should supply with necessary spares and accessories. 12. Should operate on mains 220-240Vac, 50 Hz single phase.

Fumigation Dispenser

1. Should be suitable for fumigation in Operation Theatre and other sterile clinical areas. 2. Should have a consistent particle size generation of less than one micron. 3. Should have a maximum throughput of 4 meters in a closed room. 4. Should have a vortex type design, non-rotating and non-clogging nozzle assembly. 5. Should have tough and corrosion-resistant powerhead housing. 6. Should have a chemical solution tank of minimum capacity 5 liters. 7. Should have a tough and corrosion-resistant tank. The bolts, nuts, and washers used inside the tank should be stainless steel/brass/ corrosion-resistant material. 8. Should have an easy to clean, detachable and non-corrosive chemical solution tank. 9. Should have primary and secondary filtration for the air intake system. 10. Should be compatible with a wide range of disinfectants. 11. Should operate from 200 to 240Vac, 50 Hz input supply. 12. Should have a timer device 13. 200ml solution should sterile 1000CFT area. Certification proof should be attached along with the technical bid. 14. Should have a safety certificate from a competent authority CE issued by a notified body registered in the European commission/ FDA (US)/ STQC CB Certificate/ STQC S Certificate or a valid detailed electrical and functional safety test report from ERTL. Copy of the certificate/ test report shall be produced along with the technical bid.

Suction Apparatus

1. Rating of Motor – continuous 2. Motor – thermally protected 3. Valves – Stainless steel 4. Filter – Bacterial filter autoclavable/ reusable 5. Suction Bottle Capacity - 2 x 2000 ml minimum (with safety valve) 6. Gauge - 0 to 760 mm Hg 7. Vacuum Maximum - 660 mm Hg. 8. Pump – Oil free Twin headed Piston pump 9. Suction Tubings - ID 7 mm, 5m long and non-collapsible. 10. Should have air tight lids interconnected with both jars. 11. Should have a noiseless Operation 12. Should provide filter to absorb moisture and water particles entering into the rotor. 13. Should have a safety valve to prevent entry of fluids into machine in case the suction jar fills up. 14. Should be well-designed, cabinet made of Stainless Steel 304 Grade. 15. Should have facility to adjust suction pressure. 16. Should bear ISI / CE mark 17. Should operate from 200 to 240Vac, 50 Hz input supply

Syringe pump

1. Should be easy to use and nurse friendly with drug library and dose calculation. 2. Should have automatic syringe size and model detection. 3. Should have large format LCD/TFT Display. 4. Should have a minimum flow rate range from 0.1-1200 ml/hr for 50ml syringe, 0.1- 100 ml/hr for 20ml syringe and 0.1-60ml for 10ml syringe. 5. Syringe range from (5 – 50) ml. 6. Should have a flow rate accuracy of ±2%. 7. Should have a bolus rate up to 1000 ml/hr for 50ml syringe. 8. Should have automatic and manual bolus. 9. Should have atleast 3 levels of programmable occlusion pressure. 10. Should have automatic bolus reduction system to avoid accidental bolus delivery after occlusion incident. 11. Should have a rechargeable battery with backup time of minimum 4 hours 12. Pump must trigger following alarms with visual indication:- i. Occlusion pressure alarm ii. KVO or 3 min pre-alarm iii. Syringe empty and volume infused alarm. iv. Internal malfunction and battery charge low alarm v. Syringe disengaged and incorrectly placed alarm vi. Alarm loudness control vii. No mains 1. Should work with input 200 to 240V AC 50Hz supply 2. Should have safety certificate from a competent authority CE issued by a notified body registered in the European commission/ FDA (US)/ STQC CB Certificate/ STQC S Certificate or valid detailed electrical and functional safety test report from ERTL. Copy of the certificate/ test report shall be produced along with the technical bid

SPINE ORTHOSIS AND PROSTHESIS