Queries raised by the prospective bidders

Transcription

1 PRE-BID CLARIFICATIONS / AMENDMENTS IN RESPONSE TO QUERIES RAISED BY PROSPECTIVE BIDDERS IN THE PRE-BID MEETING HELD ON , 11 AM IN THE TENDER HALL, OSMCL FOR THE TENDER OF SUPPLY & INSTALLATION OF ICU EQUIPMENT [Bid Ref. Nos. : OSMCL/ /EQUP-ICU(Cat.I)/01, OSMCL/ /EQUP-ICU(Cat.II)/02, OSMCL/ /EQUP-ICU(Cat.III)/03 Total No. of prospective bidders/ representatives present in the pre-bid meeting : 62 The queries raised by the prospective bidders on the above mentioned tender references are discussed and the following decisions were made: A) TENDER Ref. No. : OSMCL/ /EQUP-ICU(Cat.I)/01: CATEGORY- I Sl. 1 2 Item Name Blood Gas Analyser (Catridge Based) Blood Gas Analyser (Liquid Based) Queries raised by the prospective bidders Multi use cassettes may be used instead of Single use cassettes. The parameter "so 2, Hb, Hct" may be incorporated under calculated parameters. Parameters like nca++, ch+, O 2 ct, BB may not be available in most of the cartridge based system. May have BUN (Urea) / Creatinine in measured parameter. Comfort sampler under Sampling devices may be deleted. Clarification /Amendment in response to the queries Multi use cassettes / Single use cassettes may be used. The parameter "SO 2, Hct" should be in either in measured or calculated parameters. However, thb should be in measured parameters Parameters like ch+, O 2 ct, BB should not be mandatory. However, nca++ is mandatory. Should have BUN (Urea) in measured parameters. However, Creatinine is optional. Sampling device should be syringe/capillary/other. Cost of cartridges for 100 tests per month for 6 years of all parameters must be quoted separately in financial bid as mentioned in BoQ. Continuous reagent level monitoring may not have graphic display. Data may be printed in in-built or integrated printer. May not have built in auto quality control facility. Should have continuous reagent level monitoring. Data should be printed in in-built or integrated graphic printer. Should have provision for quality control free of cost as & when required by the user during Pre-bid Clarification / Amendment Page 1

2 3 Advanced Anaesthesia Workstation May have Glucose / Lactate in measured parameters. The parameter "Cl - " may be incorporated under measured parameters. warranty & CMC period. The parameter "Cl - " should be in measured parameters or the machine should have the capability to measure Anion Gap. Cost of cartridges for 100 tests per month for 6 years of all parameters must be quoted separately in financial bid as mentioned in BoQ. May be USFDA or CE (Notified) approved product. Display may be 6.5 inch instead of 8 inch. May have manual fresh gas flow setting instead of digital flow setting. May have 2 no. of pin index yokes each for O 2 & N 2 O Pressure support may be included as standard. CPAP may not be mandatory. Desfluorane vaporiser may not be required & not commonly available. PEEP level may be 1 to 20 mbar instead of 0 to 20 mbar. Monitor display size may be 18 inch or more instead of 15 inch. Provision of wireless LAN in patient monitor may not be as standard. 4 Boyle's Machine ISO may be added. Should have colour TFT/LCD display of 6.5 inch or more. Should have both manual and digital fresh gas flow setting with display. Should have additional mox connection (2nos.) for back up O 2 cylinder. Pressure support mode should be there as standard. CPAP mode is not required. Desfluorane vaporiser is not required. Hence should not be quoted. PEEP range: 3 to 20 mbar. The line "Provision for using wireless LAN card with power off storage function" is deleted. In addition to the other standards specified, the Manufacturer should be ISO certified for quality standards Pre-bid Clarification / Amendment Page 2

3 5 BIPAP (Invasive) Machine IS or ISO 5358 may be deleted. Respiratory rate may be 5 to 40bpm instead of 5 to 60bpm. Inspiratory time (T i Max.) may be 0.5 to 3 instead of 0.1 to 4 sec. Rise time ( ms) may be changed & Fall time may not be specified. Tidal volume may be 200 to 1500ml. instead of ml. Battery back up may be unto 2 hrs. instead of 4hrs. Respiratory rate should be 5 to 40bpm or above. Inspiratory time (T i Max): 0.5 or less to 3 sec. or more. Rise time: Min 100 to 600ms. or more. Fall time: ms is deleted. Tidal volume: 200ml. or less to 1500ml. or more Should have internal battery back up for minimum 2hrs. 6 Bubble Machine CPAP FiO 2 & SPO 2 monitoring may not be integrated. All the components of the machine may not have USFDA certification. IEC may not be required for this item. Compressor may have electronic dryer to avoid humidity in output air. Pressure display may not be required. Battery back up may be for 3 hrs. instead of 6 hrs. Size of nasal prongs may be specified with quantity. Should able to provide FiO 2 & SPO 2 monitoring. The major components of bubble CPAP like Air-Oxygen blender, Humidifier & Medical air compressor should be USFDA & CE (Notified body) approved. Any other component except these should be USFDA or CE (Notified) approved. Should have IEC for electrical safety. EN/IEC standard is deleted. Pressure display is not mandatory. Should have battery back up for minimum 3 hrs. except the air compressor. Should supply 6 different size of nasal prongs as per the weight category of 5 nos. each with the Pre-bid Clarification / Amendment Page 3

4 machine. 7 Central Station Monitoring Accessories : Reusable Humidifier & bubble generator Jar : 2 Nos. May have single use water chamber. Size of bonnet may be specified with quantity. Central monitoring station may be incorporated with the High end patient monitors. Required computer system may be server type. Accessories: Reusable Humidifier jar: 2nos. & bubble generator Jar: 2 Nos. should be provided. Reusable heated wire humidified patient circuits compatible with the supplied humidifier: 2nos. Should supply 3 different size of bonnet as per the weight category of 2 nos. each with the machine. Patient interface: 2nos.should also be provided. Clarification It is compulsory for the bidder to quote for both Central Station Monitor as well as Multipara Monitor (High end) in the respective row against these items in the price BoQ (as separately mentioned in BoQ) as per tender format. However the final evaluation price shall be made based on the total quantity of requirement of both the items mentioned in the tender. Example : Total evaluated price = [(Total evaluated unit price of central station x 6) + Total evaluated unit price of Multipara monitor (High end) x 52]. Based on the above evaluation criteria, the lowest evaluated bidder shall be decided. Should provide the required server based system of latest generation with suitable software for central monitoring. Pre-bid Clarification / Amendment Page 4

5 8 CPAP Machine Wireless connection between Bed to bed & Bed to CMS may be specific and capability to change monitor setting may not be recommended. Information of minimum 10,000 patients with trend may not be possible. Point no. 10 may not be required. Power backup may be required in case of power failure May have product standard of ISO instead of ISO Available modes may be generalised. Flex or equivalent comfort feature may be added. Should have only wired connection between bed to bed & bed to CMS through hospital LAN only. No wireless connection is required. Should store patient trend data for 48 hours or more. Ability to receive & display information from ancillary devices is not required. Hence Point no.10 is deleted. Adequate on line UPS for server system & 2 CMS monitor for 2 hours power back up should be provided. Should comply to EN/ISO , Particular requirement for Sleep apnea breathing therapy equipment. Should have Manual & Auto mode for CPAP. Should have flex or equivalent feature for comfortable exhalation. May not have 4 level altitude compensation. Should have leak compensation & automatic altitude adjustment. 9 Defibrillator Monitor with Sound level may be 30dB instead of 27dB. Should be USFDA or CE Approved May have synchronized & asynchronized cardio version. May have 200J in AED mode. CPR feedback may be deleted. Display type & size may be specified. Sound level should be 30dB. Should have synchronized & asynchronized cardio version with CPR feedback or equivalent. CPR feedback or equivalent feature should be provided. Should have color LCD display of minimum 6 inch diagonally. Pre-bid Clarification / Amendment Page 5

6 Non invasive pacing should be there as a standard provision. Non invasive pacing should be there as a standard provision. Charge time may be less than 7 seconds instead of 5 seconds. Charge time should be less than 7 seconds for maximum energy. CPR pad & AED pad numbers may be specified. Should provide 2 set of CPR pad/sensor and AED pad (Adult & Paediatric) of 10 nos. of each size. Standrad scope of supply may be specified. Standard supply should be as follows: 1. Paddles (Adult & Paediatric): 1 each 2. CPR pad/sensor: 2 Set 3. AED pad (Adult & Paediatric): 10 nos. of each size lead ECG cable: 1no. 5. ECG paper : 10 rolls 6. Defibrillator Carry case Supply under upgradability: lead ECG cable: 1no. 2. SPO 2 finger probe (Adult & Paediatric): 1no. each 3. SPO2 ear probe: 1no. 10 Haemodialysis Machine May be USFDA or CE approved product. Colour Display may be 10.4 inch or more instead of 12 inch May be either touch screen or touch button display. However the price for standard & upgradable features should be quoted in the price BoQ with breakup cost in the PDF file as asked in the price BoQ, which shall be taken into account for evaluation. Colour display : 10 inch or more Should have provision of touch screen or touch button. Variable diasylate flow may be ml. instead of 300 to 800ml. Blood pump flow rate may be 10 to 500ml. instead of ml. Pre-bid Clarification / Amendment Page 6

7 11 12 ICU bed manual with Bedside locker ICU bed motorised with Bedside locker 13 Infusion Pump May have inlet water flow as required by the machine. Programme profiling and basic ringe & disinfection methods may not specified in 6 steps. May have real time KT/V monitoring. Ultrapure dialysis fluid filter may be required for running the machine. Heat disinfection may be specified to 80 degree C instead of 50-80degreeC. Minimum height may be 490mm instead of 470mm. Remote hand control & Nurse hand control may not have power on indication. May have both manual / digital degree indicator. Upper & lower bed frame should have same type of framework. Castor size may be 150mm & may be of double castor type. The features relating to point no. 9, 13 & 14 may be deleted. Product may have both USFDA & CE (Notified). Should have inlet water flow as much as required by the machine. Programmable profiling (Under Point no.13) & Basic ringe & disinfection methods (Under Point no.33) should not have provision to set, store & select in 6 steps. Under point no. 19 Any additional filter / disposable filter required for running the machine should be supplied free of cost with the machine during the warranty & CMC period. Should have heat disinfection at 80 degree C with auto programming. Variable height should be from approx. 490 mm to 700 mm (Without mattress). Power-on indication on Remote hand control & Nurse hand control is not mandatory. Degree indicator should be either manual or digital. The upper & lower bed frame should be same type of framework as per the dimension & thickness mentioned in the specification. Should have double swivel wheel castor of 150mm size with high grade synthetic grip with central & directional locking mechanism with foot pedal brakes on two wheels. Quoted product should have USFDA & CE (Notified). Pre-bid Clarification / Amendment Page 7

8 Ward name, Secret code & Air bubble size may be removed from configuration. Flow Rate may be ml/ hour with no micro infusion Accuracy : ± 10% instead of ± 2% Under Configuration, the points such as "Ward name, Secret code & Air bubble size" is deleted. May be upgradable to main stream / micro stream instead of only mainstream EtCO 2. Display may be 17 inch instead of 12 inch. May have facility of viewing atleast 6 waveforms instead of 8 waveforms. SPO 2 measurement technology may be mentioned. May have 10/12 lead ECG cable for measurement. Patient monitor should be upgradable to dual IBP & main stream / micro stream EtCO 2. The pulse oximetry module should be of Masimo / Nellcor technology which should work on low perfusion & motion. Should have 10 / 12 lead ECG cable for ECG measurement. 14 Multipara (Basic) Monitor Scope of supply under standard & upgradability may be specified. All the following accessories should be under standard scope of supply: 1. NIBP Cuff (Pre term, Term Neonate, Infant, Paediatric, Adult) with hose 2 No. each Lead lead ECG Cable Paediatric (Complete Set) - 01 No. 3. SPO 2 Probe (Adult, Neonate, Paediatric) - 01 No. each (Y sensor) 4. Temp. Probe : 1 No. each for Skin & Rectal Supply under upgradability: 1. Dual IBP probe : 1 no. 2. IBP transducer (disposable): 10nos. 3. Mainstream/Microstream EtCO 2 probe with adapter: 1no. However the price for standard & upgradable features should be Pre-bid Clarification / Amendment Page 8

9 quoted in the price BoQ with breakup cost in the PDF file as asked in the price BoQ, which shall be taken into account for evaluation Multipara (High end) Patient System Monitor Warming May have 8 waveform instead of 12 waveform May have 96 hrs. review data with trend instead of 24hrs. Monitor battery back up may be through internal battery/ups. May not have hour meter. Alarm feature may be added. Should have minimum 48 hrs. review data with trend. Should have power back up for minimum 60 minutes with internal battery/ups. Hour meter is not mandatory. Should have alarm for over temperature, hose disconnect. 17 Single Syringe Pump & Dual Syringe Pump May be USFDA & CE approved product. Flow rate may be from 0.01ml to 1200ml/hr. instead of 0.1 to 1500ml/hr. May have provision to use 5cc syringes. Type of accuracy may be specified. Battery back up may be required more. Quoted product should have USFDA & CE (Notified). Flow rate should be from 0.01ml. to 999.9ml. Disposable syringes of 2cc, 5cc should also be used along with all other asked sizes of syringes with the machine. Clarified Accuracy should be ±2% with the recommended syringe, which should be specified in tender. Should have battery back up for minimum 4 hrs. Bolus function may be manual & programmable. Bolus operation should be manual & programmable upto approx.500ml.with infuse volume display. Pre-bid Clarification / Amendment Page 9

10 Flow rate & flow volume retention may be available only on stand by condition instead of power off. The item name may be corrected. Tidal volume may be 2 to 200ml. instead of 2 to 2000ml. May not have built in color touch screen display. Should retain flow rate & total infusion volume setting when the machine is in stand by mode. The item name should be spelled as Critical care Ventilator (Neonate to Infant) Tidal volume: 2 to 200ml. Should be a dedicated neonatal ventilator. Volume mode ventilation is not mandatory. Should have color touch screen display of minimum 12 inch. Inverse ratio ventilation may be generalized. Should have inverse ratio ventilation or equivalent mode. 18 Critical care Ventilator (Neonatal to Paediatric) Apnea back up ventilation may be auto or manual. May have ultrasonic/pneumatic nebuliser. Occlusion pressure may be deleted. Apnea back up ventilation should be auto or manual with apnea detection alarm. Should have inbuilt/integrated nebuliser to deliver particle size of less than 3 micron. The display parameter as "occlusion pressure" is deleted. Air compressor flow rate may not required to specify. Air compressor flow should be as per the ventilator requirement for all modes & setting ranges. NIV for BIPAP may be deleted. Should have Non invasive ventilation. BIPAP is deleted. Expiratory cassettes/valve, O2 sensor & flow sensor may be covered under warranty. HME filter may not be required for neonates. Expiratory cassettes/valve, O2 sensor & flow sensor should be covered under warranty & CMC period. HME filter is deleted under standard accessories. Pre-bid Clarification / Amendment Page 10

11 UPS may be provided instead of CVT or servo stabiliser. May be USFDA or CE approved product with country of origin of Europe, Japan or USA. NIV for BIPAP & CPAP may be deleted. Automode or equivalent mode may be provided. UPS for whole ventilator system including air compressor is not required. However should have internal battery back up for ventilator should be provided for atleast 60 minutes. Should have Non invasive ventilation. BIPAP & CPAP is deleted. Should have automode or equivalent mode. 19 Critical care Ventilator (Paediatric to Adult) Breathing rate under CMV & SIMV may be 4-80bpm. Equivalent mode for pause time may be available. May have pressure or flow trigger upto 2lpm. May not have separate interface & ventilation unit for flexible positioning. Waveform for CO2 conc. time may be deleted as EtCO2 has not been asked. May have ultrasonic/pneumatic nebuliser of suitable particle size. Pressure-Volume loops is asked 2 times. Air source type may be clear out. Breathing rate should be 4-80bpm. Pause time: 0 to 70% of breath cycle time or equivalent parameter should be available. Should have pressure or flow trigger upto 2 L/min. Deleted this line under point no. 6 Deleted the CO2 conc.time under point no.12. Should have inbuilt/integrated nebuliser to deliver particle size of less than 3 micron. Under point no. 13, deleted the repeating Volume-Pressure loop. Clarified Should provide air supply automatically during loss in central air supply through compressor/ turbine (Not blower/piston). In case of internal air source through compressor, the original manufacturer (OEM) should be Pre-bid Clarification / Amendment Page 11

12 21 Transport Ventilator May be asked either permanent or disposable flow sensor. Expiratory cassettes/valve, O2 sensor & flow sensor may be covered under warranty. UPS may be provided instead of CVT or servo stabiliser. May be revised as per requirement and may be incorporated with MRI compatibility. MR compatibility or MR conditional upto 3Tesla may be useful during MRI scanning. same as the ventilator & should be USFDA & CE approved. Under standard accessories: Should supply permanent O2 sensor: 1no. or disposable sensor (O2 cell) : 10nos. to be supplied through out warranty & CMC period. Expiratory cassettes/valve, O2 sensor & flow sensor should be covered under warranty & CMC period. UPS for whole ventilator system including air compressor is not required. However should have internal battery back up for ventilator should be provided for atleast 60 minutes. Revised detail specification is attached at Annexure-A Incorporated in revised specification. B) TENDER Ref. No. : OSMCL/ /EQUP-ICU(Cat.II)/02: CATEGORY- II Sl. Item Name Queries raised by the prospective bidders 1 Blood/Fluid Warming System KVO rate may be as per fluid flow requirement. May have highly conductive heating plate technology to disperse heat. May have test check facility. Alarm feature may be added. Clarification /Amendment in response to the queries The point "KVO to 20,000ml/hr. with one warming unit" is deleted. Should have auto/manual test check facility. Should have audio/visual alarm for high/low temp. & disposable disconnection. Pre-bid Clarification / Amendment Page 12

13 Injection port may be provided with the machine. Disposable injection port should be provided with the consumable tube/catridge. May have USFDA & CE approved product. 2 ECG Machine (6 Channel) Size of printer paper may be specified. Should record ECG on thermal printer of A4 size paper. Memory for recording ECG may be less. Should have memory to record ECG of minimum 30 patients. May have alphanumeric keyboard or touch screen panel for entering patient information. Should have alphanumeric elastomer keyboard or color touch screen panel for entering patient information. 3 ECG Machine (12 Channel) Display of the machine may be specified. Display size should be minimum 6 inch or more. Sampling rate may be 1000s/sec/ch. instead of 5000s/sec/ch. Digital sampling rate should be minimum 1000samples/sec/channel. 4 Foetal Monitor (CTG Machine) May have USFDA & CE approved product. May have noise filtering facility. Should have noise filtering facility. 5 RO Water Treatment Plant May be manual RO system instead of microprocessor based to perform under high humidity condition. Raw water tank type must be specified. RO treatment process may be specified. Should be skid mounted panel linked manually operated double filtration RO system. Raw water tank should be made of HDPE having 12,000ltr.capacity.(Sintex/Oriplast/oth er reputed make) Should have process chambers for Oxidation, Chlorine dosing system, Multigrade filter, Activated carbon filter, Water softner, Anti scalant dosing system, UV steriliser. (Capacity of each process chamber should be specified.) Pre-bid Clarification / Amendment Page 13

14 SS grade of RO storage tank may be specified. May have double post RO storage tank with different permeate flow. Pre RO micron filter type may be specified. RO water storage tank should be made form stainless steel of SS-316 grade. Should have 1st post RO storage tank of 3000ltr.capacity of SS-316 and 2nd post RO storage tank of 1500ltr.capacity of SS-316 with internal plumping by food grade UPVC pipe between the two tank. Should have Pre RO filter of 0.1 micron for bacterial protection. ph meter may be added as measuring tool. RO feed pump type may be specified. May have loop line for returning of excess water to premeate tank. Plited catridge filters may be required at dialysis inlets. Should have online ph meter along with other asked measuring tools. Should have RO feed pump of 0.5HP of Kirloskar/ Crompton/ CRI/other reputed make with feed filter having flow of 2000LPM or higher. Should have loop line system for returning of excess water to premeate tank to avoid wastage. Should be provided with plited catridge with MF housing at every inlet of dialysis unit or any other required machines. May have provision for 2nos.of 5L oxygen cylinder instead of 10L cylinder. Should have provision to attach two 5L oxygen cylinder. Empty cylinders is not required. Hence the cost of the same need not be quoted. 6 Radiant Warmer with Basinet Cylinder provision may not be required. Should have provision to attach two 5L oxygen cylinder. Empty cylinders (2nos.) is not required. Hence the cost of the same need not be quoted. May have fixed basinet. Castor size of basinet may be 5cm instead of 10cm. Basinet castor size should be 5cm or above with locking system. Pre-bid Clarification / Amendment Page 14

15 Quartz type heater may be asked. Should have Ceramic/Calrod/Quartz heater. Under Point no.7, The word "No Air" is deleted. Hence air sensor should be provided. Temp. setting range may be maximum upto 38degreeC as per IEC Temperature setting range should be 32 to 38 degreec. Basinet may be made of polycarbonate or acrylic with mattress. Basinet should be made of polycarbonate or acrylic (transparent) with mattress. Temp. accuracy may be 1 degreec instead of 0.2 degee C. More alarm features may be added like sensor disconnect / malfunction. Added Should have alarm for sensor disconnect/sensor malfunction along with all other asked alarms. Basinet tilting angle may be upto 12 deg. Basinet should have tilting angle upto 12deg. 7 8 Phototherapy Unit (Single Surface & Double Surface) Suction Machine (Electrical & Foot operated) IEC may be removed. Height of light source may be fixed. Irradiance level may be adjustable. Manufacturer may not match to turnover criteria. These two items shall be considered under Category-III and shall be evaluated as per the specified turnover criteria. However, as there cannot be any change in the price BoQ due to e- tender, the bidder shall quote the price in relevant row under price BoQ as per the format in category-ii. Pre-bid Clarification / Amendment Page 15

16 C) TENDER Ref. No. : OSMCL/ /EQUP-ICU(Cat.III)/03: CATEGORY- III Sl. Item Name Airbed (Low end) & Airbed (High end) Ambu (Silicone) Fumigation Machine Bag Queries raised by the prospective bidders Mattress may have standard manufacturer warranty of 1year. ETO sterilisable may not be required. May not have 3 yrs. of manufacturer warranty It may be an obsolete technology. Fogger may be used instead of fumigator. 4 Cidex Tray Material may be specified. 5 6 Laryngoscope Set (Adult & Paed./Neonate) IEC may not be required for these items as it run through internal battery. May have fibre optic technology with LED light. Quality Certification : ISO & OHSAS may be deleted for furniture items. Clarification /Amendment in response to the queries Only mattress should have manufacturer warranty of 1yr. ETO sterilisable is not required. Hence the point is deleted. Should have 1yr.of standard manufacturer warranty or 100 autoclave cycle. Fumigator machine shall be replaced as Fogger machine. Detail specification is attached at Annexure-A Should be made of glass filled polypropylene having inner perforated tray with top cover. Under product quality standard, IEC standard shall be deleted. Hence not required for these items. Should have fibre optic technology with LED light. There should be a freely moving light intensifier of light from the light source through to the tip of the fiber optic blade to prevent any possibility of cross contamination. D) General Terms & Conditions 1 BG/DD may be accepted as EMD. 2 Alternate bidding from two different manufacturers may be allowed. Alternate bids are not allowed. Pre-bid Clarification / Amendment Page 16

17 3 4 Delivery period may be extended up to 75 days instead of 60 days. Performance bank guarantee may be permitted from date of installation. Other Clarifications 1. Under Product Quality Standards of the respective items: The standard mentioned as ISO/IEC is corrected as EN/IEC The particular requirements of the individual items for EN/IEC as mentioned will remain same. 2. Refurbish product or model shall not be supplied. The supplier shall furnish the New Machine Manufacturing Certificate from the Original Equipment Manufacturer along with import data with machine serial number (In case of import from foreign) during time of supply. N:B 1. The amendments mentioned above are to be treated as amendments in the technical specification(s) and term(s) and condition(s) of the above tender reference. All other technical specifications and terms conditions remain unchanged. 2. Since any text in the price BOQ can t be changed in the e-tender portal, the amendments mentioned in the specifications above are to be treated as amendments in the price bid/ BOQ also. Pre-bid Clarification / Amendment Page 17

18 TRANSPORT VENTILATOR Product Quality Standards: Should be USFDA and CE (Notified body) approved model. Manufacturer should be ISO certified for quality standards. Should comply to EN/IEC for electrical safety. Technical Specification: Should be microprocessor controlled, portable, light weight. Should operate with main electric supply as well as with battery. Annexure -A Should be able to work both with cylinders and central pipeline. Connectors and high-pressure tubing of appropriate length to be supplied. Should have turbine technology for supplying air- oxygen mixture. Should have following modes of ventilation like CMV, Assist control, PS- PEEP. Should have automatic leakage compensation. Should be MRI conditional upto 3 Tesla, 430G/cm. Audio-visual alarms for High/low oxygen pressure Leakage/disconnection Power failure Apnea Low battery Should have following settings Tidal Volume: ml PEEP/CPAP & PS RR up to 40bpm I: E ratio: 1:3 to 2:1 FiO 2: 50 to 100% Rechargeable batteries. Should fix on rails of patient bed through hinged support & transport trolley with wheels. Trolley of same make of ventilator should be provided with the machine. Should supply two sets of reusable silicone ventilator circuits. Must have minimum 4hrs. of power backup with internal battery. Should capable to operate in various environments such as Emergency, Ambulance, Aircraft, Hospital & MRI room. Ventilator should be upgradeable to volumetric CO2 & SPO2 monitoring in same screen. [Price is upgradability with required patient probes should be quoted separately in the specified format of BoQ.] Pre-bid Clarification / Amendment Page 18

19 Power supply: Power input to be V AC, 50Hz fitted with Indian plug of appropriate rating. Warranty: Should have 3yrs. of manufacturer warranty. FOGGER MACHINE Product Quality Standards: Manufacturer should be ISO 9001 certified. Product must be CE/BIS certified. Technical Specification: Should generate ultra fine & non wetting aerosol (Dry vapour type) of size upto 5-10 micron. Should be light weight, portable. Should cover minimum 10,000cu ft. of area. Should provide sufficient contact time with no flood of disinfectant on floor/surface. Should have mirror polished inner surface SS 304 tank. Should be shock proof motor housing made of unbreakable high grade engg. plastic. Should have adjustment for low & heavy fogging. Should have non clogging nozzle assembly with stainless steel needle. Should have two layer sof filters for dust & fog separation. Should be compatible with wide range of disinfectants or fumigant solutions. Power supply: Power input to be V AC, 50Hz fitted with Indian plug of appropriate rating Warranty: Should have 3yrs. of manufacturer warranty. Sd/- Managing Director, OSMC Pre-bid Clarification / Amendment Page 19