rate contract of consumable items for GMERS General Hospital Himatnagar

Products Specification

SR NO. NAME OF INSTRUMENT SPECIFICATION Pack of

1 AIR OXYGEN BLENDER  The blender should have dual integrated flowmeter.  Dial for Fio2 setting (21 to 100 %)  Left Flowmeter Range 3-15 lpm. (1-15 lpm. if bleed is on)  Right Flowmeter Range 0.0-1.0 lpm., 0.0-3.5 LPM. or 1-15 lpm(with 3 lpm bleed on)  Accuracy ±3% full scale  The blender should be US FDA approved.  It should be mounted on mobile pole with castors.  The blender should be suitable for low flow oxygen, bubble CPAP and Nasal high flow oxygen therapy.  US FDA and CE approved Pack of 1

2 Water Trap  Filter Trap Pack of 1

3 Bubble C-pap circuit for new born. BC161  The patient heating circuit should have integrated spiral heated coil for uniform heating.  The delivery system should have Maximum Input Flow- 15L/min and maximum mean CPAP- 15cmH20.  Humidification chamber should be auto feed with dual float system  Chamber Compressible volume 260- 300 ml  Max peak flow should be 180ltr/min.  CPAP Bubble generator should have adjustable probe for pressure settings 3-10 cm of H20.It should have detachable overflow container to maintain constant water level. Volume for generator ~ 500ml.  The system should have safety mechanism with pressure relief valve and ports for pressure and Fio2 monitoring. Pressure relief should be 17 cmh20 and above @8L  US FDA and CE approved BOX OF 10

4 INFANT BONNET BC300  Made of Nylon/cotton blend.  Has straps on either sides for securing nasal tubing.  Has option of open top for performing head ultrasound.  Has foam block strap on forehead for sung fit of nasal tubing.  sizes17-22cm BC300.  US FDA and CE approved BOX OF 5

5 INFANT BONNET BC303  Made of Nylon/cotton blend.  Has straps on either sides for securing nasal tubing.  Has option of open top for performing head ultrasound.  Has foam block strap on forehead for sung fit of nasal tubing.  Sizes:22-25cm BC303  US FDA and CE approved BOX OF 5

6 INFANT BONNET BC306  Made of Nylon/cotton blend.  Has straps on either sides for securing nasal tubing.  Has option of open top for performing head ultrasound.  Has foam block strap on forehead for sung fit of nasal tubing.  Sizes: 25-29cm BC306  US FDA and CE approved BOX OF 5

7 INFANT BONNET 309  Made of Nylon/cotton blend.  Has straps on either sides for securing nasal tubing.  Has option of open top for performing head ultrasound.  Has foam block strap on forehead for sung fit of nasal tubing.  Sizes :29-36cm. BC309  US FDA and CE approved BOX OF 5

8 NASAL PRONGS– IN FANT CPAP. BC3020  Should be short Bi-Nasal.  Made of Silicone.  Fit snugly in the nare.  Available in different sizes based on nare diameter and width of septum.  Should be compatible for use with nasal tubing with glider technology.  Size BC3020  US FDA and CE approved BOX OF 10

9 NASAL PRONGS– IN FANT CPAP. BC3520  Should be short Bi-Nasal.  Made of Silicone.  Fit snugly in the nare.  Available in different sizes based on nare diameter and width of septum.  Should be compatible for use with nasal tubing with glider technology.  Size BC3520  US FDA and CE approved BOX OF 10

10 NASAL PRONGS– IN FANT CPAP. BC4030  Should be short Bi-Nasal. Made of Silicone.  Fit snugly in the nare.  Available in different sizes based on nare diameter and width of septum.  Should be compatible for use with nasal tubing with glider technology.  Size BC4030  US FDA and CE approved BOX OF 10

11 NASAL PRONGS– IN FANT CPAP. BC4540  Should be short Bi-Nasal.  Made of Silicone.  Fit snugly in the nare.  Available in different sizes based on nare diameter and width of septum.  Should be compatible for use with nasal tubing with glider technology.  Size BC4540  US FDA and CE approved BOX OF 10

12 NASAL PRONGS– IN FANT CPAP. BC5040  Should be short Bi-Nasal.  Made of Silicone.  Fit snugly in the nare.  Available in different sizes based on nare diameter and width of septum.  Should be compatible for use with nasal tubing with glider technology.  Size BC5040  US FDA and CE approved BOX OF 10

13 NASAL PRONGS– IN FANT CPAP. BC5050  Should be short Bi-Nasal.  Made of Silicone.  Fit snugly in the nare.  Available in different sizes based on nare diameter and width of septum.  Should be compatible for use with nasal tubing with glider technology.  Size BC5050.  US FDA and CE approved BOX OF 10

14 NASAL MASK- Infant Nasal CPAP. BC800  Made of Soft silicone material.  Anatomically shaped for better fit and easier sealing.  Requires less force to seal.  Compatible to use with nasal tubing with foam block and glider technology.  4 different sizes- Small BC800  US FDA and CE approved BOX OF 10

15 NASAL MASK- Infant Nasal CPAP. BC801  Made of Soft silicone material.  Anatomically shaped for better fit and easier sealing.  Requires less force to seal.  Compatible to use with nasal tubing with foam block and glider technology.  4 different sizes - Medium BC801  US FDA and CE approved BOX OF 10

16 NASAL MASK- Infant Nasal CPAP. BC802  Made of Soft silicone material.  Anatomically shaped for better fit and easier sealing.  Requires less force to seal.  Compatible to use with nasal tubing with foam block and glider technology.  4 different sizes – Large BC802  US FDA and CE approved BOX OF 10

17 NASAL MASK- Infant Nasal CPAP. BC803  Made of Soft silicone material.  Anatomically shaped for better fit and easier sealing.  Requires less force to seal.  Compatible to use with nasal tubing with foam block and glider technology.  4 different sizes - Extra Large. BC803 BOX OF 10

18 NASAL TUBING for INFANT CPAP BC 191  Made of flexible breathable membrane and doesn’t allow kinking.  Has Glider technology with hooks on either sides that allows easier repositioning of nasal prongs and fixation of side straps in bonnet.  Has dense foam block with tear off strips to secure the nasal Tubing on baby’s forehead.  Resistance to flow nasal tubing. o 50mm: 0.49cmH20@ 6l/min. o 70mm: 0.53cmh20@ 6l/min.100Mm o 0.55cmh20@6l/min.  Has Sizing guide for selecting size of Nasal prongs and mask  Based on nare diameter rand septum width.  Size -70mm. BC 191  US FDA and CE approved Box of 5

19 GAS LINEBC402 Gas Supply Line Two Flow Meter For Bubble CPAP US FDA and CE approved Box of 5

20 Breathing circuit for Heated Humidified High Flow Nasal cannula ventilation – NICU.RT330  Patient circuit should be light weight with integrated spiral heating coil for uniform heating.  The tubing should have insulation sheath to minimise rainout and tubing length should be at least 1.75m to facilitate feeding and Kangaroo mother care.  Auto fill humidification chamber with dual float system.  The system should have pressure relief mechanism with pop off valve.  Ports for pressure and Fio2 monitoring.  Compatible for use on preterm and neonatal nasal cannulas.  Suitable for delivery wide range of flows from 0.25 to 15 liters suitable for use on preterm and neonates.  US FDA and CE approved Box of 10

21 High Flow Nasal Cannula Preterm OJR410  The cannula should be anatomically contoured to deliver wide range of Flows to allow flexibility of treatments.  Suitable for delivering heated and humidified respiratory gases to Patient up to 25Ltr/min based on sizes of cannulas.  Made of soft material to minimize nasal trauma.  Facilitates kangaroo care and easier feeding should have hydrocolloid adhesive pads on Velcro that stick on skin to secure prongs.  Adhesive pads should be easily replaceable.  Short flexible kink free tubing.  Available sizes Preterm applications OJR410  US FDA an CE approved Box of 20

22 High Flow Nasal Cannula Neonate OJR412  The cannula should be anatomically contoured to deliver wide range of Flows to allow flexibility of treatments.  Suitable for delivering heated and humidified respiratory gases to Patient up to 25Ltr/min based on sizes of cannulas.  Made of soft material to minimize nasal trauma.  Facilitates kangaroo care and easier feeding should have hydrocolloid adhesive pads on Velcro that stick on skin to secure prongs.  Adhesive pads should be easily replaceable.  Short flexible kink free tubing.  Available in different sizes for, Neonate OJR 412 applications  US FDA an CE approved Box of 20

23 High Flow Nasal Cannula–Infant OJR414  The cannula should be anatomically contoured to deliver wide range of Flows to allow flexibility of treatments.  Suitable for delivering heated and humidified respiratory gases to Patient up to 25Ltr/min based on sizes of cannulas.  Made of soft material to minimize nasal trauma.  Facilitates kangaroo care and easier feeding should have hydrocolloid adhesive pads on Velcro that stick on skin to secure prongs.  Adhesive pads should be easily replaceable.  Short flexible kink free tubing.  Available sizes infant OJR414 applications  US FDA an CE approved Box of 20

24 High Flow Nasal Cannula pediatric. OJR416  The cannula should be anatomically contoured to deliver wide range of Flows to allow flexibility of treatments.  Suitable for delivering heated and humidified respiratory gases to Patient up to 25Ltr/min based on sizes of cannulas.  Made of soft material to minimize nasal trauma.  Facilitates kangaroo care and easier feeding should have hydrocolloid adhesive pads on Velcro that stick on skin to secure prongs.  Adhesive pads should be easily replaceable.  Short flexible kink free tubing.  Available sizes Paediatric OJR416 applications  US FDA an CE approved Box of 20

25 High Flow Nasal Cannula pediatric. OJR418  The cannula should be anatomically contoured to deliver wide range of Flows to allow flexibility of treatments.  Suitable for delivering heated and humidified respiratory gases to Patient up to 25Ltr/min based on sizes of cannulas.  Made of soft material to minimize nasal trauma.  Facilitates kangaroo care and easier feeding should have hydrocolloid adhesive pads on Velcro that stick on skin to secure prongs.  Adhesive pads should be easily replaceable.  Short flexible kink free tubing  Available sizes Paediatric OJR418 applications  US FDA an CE approved Box of 20

26 High Flow Nasal Cannula Preterm OJR410VT (VANTILATION TRANSITION KIT)  High flow national cannula ventilation transition kit.  The cannula should be anatomically contoured to deliver wide range of Flows to allow flexibility of treatments.  Suitable for delivering heated and humidified respiratory gases to Patient up to 25Ltr/min based on sizes of cannulas.  Made of soft material to minimize nasal trauma.  Facilitates kangaroo care and easier feeding Should have hydrocolloid adhesive pads on Velcro that stick on skin to secure prongs.  Adhesive pads should be easily replaceable.  Short flexible kink free tubing  Available sizes Preterm applications OJR410VT  US FDA an CE approved Box of 5

27 High Flow Nasal Cannula Neonate OJR412VT (VANTILATION TRANSITION KIT)  High flow national cannula ventilation transition kit.  The cannula should be anatomically contoured to deliver wide range of Flows to allow flexibility of treatments.  Suitable for delivering heated and humidified respiratory gases to Patient up to 25Ltr/min based on sizes of cannulas.  Made of soft material to minimize nasal trauma.  Facilitates kangaroo care and easier feeding should have hydrocolloid adhesive pads on Velcro that stick on skin to secure prongs.  Adhesive pads should be easily replaceable.  Short flexible kink free tubing  Available in different sizes for , Neonate OJR 412VT applications  US FDA an CE approved Box of 5

28 High Flow Nasal Cannula–Infant OJR414VT (VANTILATION TRANSITION KIT)  High flow national cannula ventilation transition kit.  The cannula should be anatomically contoured to deliver wide range of Flows to allow flexibility of treatments.  Suitable for delivering heated and humidified respiratory gases to Patient up to 25Ltr/min based on sizes of cannulas.  Made of soft material to minimize nasal trauma.  Facilitates kangaroo care and easier feeding should have hydrocolloid adhesive pads on Velcro that stick on skin to secure prongs.  Adhesive pads should be easily replaceable.  Short flexible kink free tubing  Available sizes infant OJR414VT applications  US FDA an CE approved Box of 5

29 High Flow Nasal Cannula pediatric. OJR 416VT (VANTILATION TRANSITION KIT)  High flow national cannula ventilation transition kit.  The cannula should be anatomically contoured to deliver wide range of Flows to allow flexibility of treatments.  Suitable for delivering heated and humidified respiratory gases to Patient up to 25Ltr/min based on sizes of cannulas.  Made of soft material to minimize nasal trauma.  Facilitates kangaroo care and easier feeding should have hydrocolloid adhesive pads on Velcro that stick on skin to secure prongs.  Adhesive pads should be easily replaceable.  Short flexible kink free tubing  Available sizes Paediatric OJR416VT applications  US FDA an CE approved Box of 5

30 High Flow Nasal Cannula pediatric. OJR418VT (VANTILATION TRANSITION KIT)  High flow national cannula ventilation transition kit.  The cannula should be anatomically contoured to deliver wide range of Flows to allow flexibility of treatments.  Suitable for delivering heated and humidified respiratory gases to Patient up to 25Ltr/min based on sizes of cannulas.  Made of soft material to minimize nasal trauma.  Facilitates kangaroo care and easier feeding should have hydrocolloid adhesive pads on Velcro that stick on skin to secure prongs.  Adhesive pads should be easily replaceable.  Short flexible kink free tubing  Available sizes Paediatric OJR418 VT applications  US FDA an CE approved Box of 5

31 Electrical Adaptor 900MR805  Electrical Adaptor  Dual Heated  RT Circuit  US FDA and CE approved Pack of 1

32 Electrical Adaptor 900MR806  Electrical Adaptor  Single Heated  RT Circuit  US FDA and CE approved Pack of 1

33 Temperature Probe MR869  Temperature Probe  Airways Temperature and flow  For use with 1.5mtr circuit  With right angle connector MR850  US FDA and CE approved Pack of 1

34 NIV Mask. (Ventilator Mask)(NIVRIO MASK)  Available in four different size extra small, small, Medium and Large.  Soft silicon cushion for effective sealing in case of gas flow, Comfortable seal and light weight.  Quick release mechanism in case of emergency  Single motion refit.  Soft and flexible headgear for superior comfort with self-adjusting crown strap.  Zones on either side of the mask minimize leak around Nasogastric / Orogastric. (NG/OG) tubes.  Dual swivel elbow for 360 rotation and minimize drag on Circuit.  US FDA and CE approved Box of 10

35 – Dual heated Neonatal Ventilator Circuit RT265  1m Inspiratory tubing with spiral heating coil for uniform heating.  Compatible for use with servo controlled heated humidifier with Ports for temperature and flow sensors for feedback mechanism.  Expiratory limb made of moisture diffusing material without Water trap.  Auto-fill humidification chamber with dual float mechanism for humidification up to 100 % Pressure line should be part of the circuit.  Suitable for bias flow and low flow ventilators.  Extension/dry line for ventilator to humidifier chamber, duel adaptor and port for NO delivery.  Adaptor for oxygen delivery using nasal cannula.  Swivel Y-piece with duck bill valve for suctioning.  US FDA and CE approved Box of 10

36 HEATED HUMIDIFIED HIGH FLOW NASAL CANNULA DEVICE 900MR850  The device should have integrated flow generator to deliver flows from 2 to 60 litres.  Integrated Air/oxygen blending and Fio2 monitoring with facility to deliver wide range of oxygen concentrations from 21 to 100 %.  Oxygen sensor does not require in field calibration.  Clinician menu for setting range of Fio2 and flow settings.  Inbuilt heated humidifier to deliver warm and humid gases to airway. The humidification chamber should have dual float with auto feed system.  Display to monitor temperature of humidified gas, flow rate and fio2 Visual and audible alarm indication for Tubes disconnect Leaks, tube blockages, and Water out and hardware fault with error codes. Audible power failure alarm.  The device should have thermal disinfection mode to minimize contamination. Heated tube for sterilization of the device should be provided with the device.  The device should have two year replacement warranty and does not require servicing.  Supply frequency: 50/60 Hz, Supply voltage: 220-240 v  Sound pressure level 45dbA@1m  Oxygen analyser accuracy +-10 % (within range of 25-80 % Fio2)  The unit should be compliance with international standards. IEC 60601 and ISO 13485 quality standard  Certification: US FDA and European CE approved  Compliant with international standards. IEC 60601 and ISO 13485 quality  Suitable for use in PEDIATRIC ICU, ICU, HDU, recovery, wards and emergency department  US FDA and CE approved 1 Pc

37 MOUNTING POLE FOR HIGH FLOW DEVICE  Hospital pole stand made of Stainless steel with sturdy base on 4 castors/wheels at least two lockable.  I.V hook for sterile/distilled water bag or bottle for active humidification.  The pole should have two integrated clamps for mounting humidifier or flow generator.  Basket for storing accessories.  Tray for mounting High flow device.  US FDA and CE approved 1 Pc

38 HIGH FLOW METER FOR OXYGEN 0-25 LTR/MINUTE  The flowmeter should be calibrated for 0-25psi pressure.  It should have durable polycarbonate housing highly accurate needle valve Adjustable knob for flow Standard DISS outlet. 3-in -1 adaptor  It should have pole mounting clamp integrated. Flow range 0-25lpm  It should have Oxygen Hose for connection to centralised Oxygen source.  US FDA and CE approved 1 NO

39 Heated humidified high flow Circuit for Paediatric 900PT561  Patient breathing tube with integrated heating coil and flow/temperature Sensor.  The circuit should be light weight to minimise drag on interface.  Flexibility to use for adult and paediatric application.  The circuit should have insulating layer to minimise condensate.  Circuits should be available with lock in system  Certification : US FDA and European CE approved Box of 10

40 Aiirvo circuit900PT562  Patient breathing tube with integrated heating coil and flow/temperature Sensor.  The circuit should be light weight to minimise drag on interface.  Flexibility to use for adult and paediatric application.Heated Breathing Tube (circuit) + MR290, AirSpiral™, Nebulizer for AIRVO 2 (Box 10)  The circuit should have insulating layer to minimise condensate.  Circuits should be available with lock in system  Certification : US FDA and European CE approved

41 DISINFECTION KIT DISINFECTION KIT FOR HEATED HUMIDIFIED HIGH FLOW NASAL CANNULA DEVICE  The kit should consist of tubing and filter.  The tubing should have integrated coil for thermal disinfection of the device  The disinfection cycle should be for 55 minutes to achieve high level disinfection  Operating conditions:  Ambient temperature: 18-30 deg. c  Ambient humidity :60 to 95 %  US FDA and CE approved 1 NO

42 AIR FILTER PT913 AIR FILTER FOR HEATED HUMIDIFIED HIGH FLOW NASAL CANNULA DEVICE US FDA and CE approved Pack of 2 Pc

43 AIRVO FILTER HOLDER PT912 AIRVO FILTER HOLDER FOR HEATED HUMIDIFIED HIGH FLOW NASAL CANNULA DEVICE US FDA and CE approved Pack of 1 Pc

44 Wiggle Pad WJR112 Wiggle Pad for Nasal Cannula: Two different size  Hydrocolloid based adhesive on Velcro.  It should be easily replaceable.  Available in two different sizes.  US FDA and CE approved Box of 20

45 T-Piece Infant Resuscitator NeoPuff  The device should be ideal for use in Labour room, NICU and during transportation.  It should be powered by gas flow with no electrical or battery operation.  It should be light weight and easy to handle.  In-built Pressure Gauge (manometer) to set & indicate delivery of PIP & PEEP  Manometer range -10 to 80cmH20 (mbar)  Peak Inspiratory Pressure ( PIP ) at 8 lpm : 3 to 72 cmH20  Positive End Expiratory Pressure ( PEEP ) at 8lpm : 0 cmH2O to 9cmH2O  Safety provision with adjustable Pressure Relief Valve for maximum limiting  Pressure. Maximum pressure relief at 8LPM : 5 to 70cm H2O  Delivered oxygen up to 100% depending on gas supply.  Unit should be compatible with neonatal mask & endotracheal tube.  The patient T –Piece should have port for surfactant delivery should be compatible for use with heated humidifier.  Spiral Heated wire circuit with integrated T- Piece compatible for use with heated humidifier should be supplied with system.  Operating and storage limits -20°C to 50°C and Up to 90% relative humidity.  The equipment should be supplied with patient tubing with attached T-piece -10 Nos  US FDA and CE approved 1 Pc.

46 KIT, ERGONOMIC, NEONATAL RESUSCITATION, WITHOUT MASK. RD1300 (NEOPUFF) CIRCUIT IS single-use, ergonomically designed T-piece breathing circuit, commonly used with the Neopuff™ Infant T-piece Resuscitator for neonatal and infant resuscitation. It is designed to provide consistent, controlled, and safe delivery of pressure to infants Box of 10

47 Dual heated Adult Ventilator Circuit. RT380  The Breathing circuit should have 1.5 m aspiratory limb with spiral heating coil for uniform tubing.  The expiratory limb should be made of moisture diffusing membrane without need for water trap.  Auto-fill humidification chamber with dual float mechanism.  0.5 m ventilator to humidifier extension.  Maximum chamber operating pressure 8kPA.  It should be suitable for Invasive ventilation, on- Invasive ventilation and Oxygen therapy.  Integrated MDI port for improved drug delivery.  Bacterial viral end expiratory filter.  US FDA and CE approved Box of 10

48 HIGH FLOW METER FOR OXYGEN 70-75 LTR/MINUTE  The flowmeter should be calibrated for 50- 70psi pressure.  It should have durable polycarbonate housing.  Highly accurate needle valve  Adjustable knob for flow  Standard DISS outlet.  3-in -1 adaptor  It should have pole mounting clamp integrated.  Flow range 0-70 lpm.  It should have Oxygen Hose for connection to centralized Oxygen source.  US FDA and CE approved 1 Pc

49 HIGH FLOW NASAL CANNULA – ADULT OPT942  The cannula should be anatomically contoured and wide bore for softer streamlined fit to deliver wide range of flows to allow flexibility of treatments.  The cannula should deliver 10 to 60 ltrs of flow.  Customizable head strap provides a secure and soft fit Breathable membrane reduces formation of mobile condensate.  Made of soft material to minimize nasal trauma.  Available in sizes for Small OPT 942,  US FDA and CE approved BOX OF 20

50 HIGH FLOW NASAL CANNULA – ADULT OPT944  The cannula should be anatomically contoured and wide bore for softer streamlined fit to deliver wide range of flows to allow flexibility of treatments.  The cannula should deliver 10 to 60 ltrs of flow.  Customizable head strap provides a secure and soft fit Breathable membrane reduces formation of mobile condensate.  Made of soft material to minimize nasal trauma.  Available in sizes for Medium OPT 944,  US FDA and CE approved BOX OF 20

51 HIGH FLOW NASAL CANNULA – ADULT OPT946  The cannula should be anatomically contoured and wide bore for softer streamlined fit to deliver wide range of flows to allow flexibility of treatments.  The cannula should deliver 10 to 60 ltrs of flow.  Customizable head strap provides a secure and soft fit Breathable membrane reduces formation of mobile condensate.  Made of soft material to minimize nasal trauma.  Available in sizes for Large OPT 946,  US FDA and CE approved BOX OF 20

52 HIGH FLOW METER FOR OXYGEN 0-25 LTR/MINUTE • The flowmeter should be calibrated for 0-25psi pressure. • It should have durable polycarbonate housing highly accurate needle valve Adjustable knob for flowStandard DISS outlet.3-in -1 adaptor • It should have pole mounting clamp integrated. Flow range 0-25lpm • It should have Oxygen Hose for connection to centralised Oxygen source. US FDA and CE approved 1 NO

53 Servo Controlled Heated Device for Ventilator/ BCPAP (Heater Base humidified - 950AXX) • Humidifier should have both Temperature and Flow Sensors. • The humidifier should have a provision for the attachment of a sensor cartridge with inbuilt sensor probes which will help detect temperature and flow of incoming gases. • It should have a touch screen LCD screen which displays the temperature of the humidified gasses being delivered at the patient end • It should have minimal assembly connections, be easy and simple to set up. • It should be suitable for Adult, Paediatric and Neonatal ventilation. • The humidifier in the adult mode should have comfort temperature settings for NIV and HFNC • NIV mode range of temperatures should ideally be 27, 29 & 31. • The HFNC mode range of temperatures should ideally be 33, 35 & 37 • It should have incoming gas temperature probe to detect temperature of incoming gases in the chamber The temperature & flow probes should not require any cleaning and sterilization. • It should have an adaptor for providing power to heat the expiratory limb of the ventilator circuit. • Option of monitoring Flow rate, Heater plate temperature, duty cycle of heater coil and heater plate on the humidifier screen. Storage temperature • Should have a storage temperature of -10 to 60 degrees Celsius Storage Humidity • 10-95% relative humidity non-condensing Display Range of Temperature • 10-50 deg Centigrade Accuracy: ± 2 degree Celsius (in 25 to 45 degrees temperature range) Humidity Performance-Adult • Invasive mode (37 °C): > 33 mg/L • Mask mode (31 °C): > 12 mg/L • Optiflow mode (37 °C): > 12 mg/L Humidity Performance- Neonatal • Neonatal mode (37 °C): > 33 mg/L Operating Pressures • Minimum of 70 kPa (equivalent to a maximum altitude of 3000 m) Operating Flow Range @ 22 degree centigrade • Invasive( 5-60 Liters/ Minute) • Non Invasive( 5-120 Liters/ Minutes) • Optiflow Range( 5-70 Liters/Minute) Warm up time • Should have a warmup time of less than 30 minutes Alarms Should have visual and audible alarms to detect circuit disconnection, no water alarm, low and high temperature alarms, Cartridge detection alarm, tube fault alarm, out of range alarm, cartridge life alarm, service required alarm etc. Sound Pressure Level • Alarms to exceed 45dBA @1m • Should be CE Approved with all international electrical and safety standards • Warranty: One year manufacturer warranty on humidifier & sensor cartridge 1 NO

54 Sensor cartridge 950s01 • Width:-168mm, • Height :-135mm, • Depth:-88mm, • Weight:-355g • Quantity per pack:- 1 each • Manufacturing mode:-Produced in a controlled working environment. • Disposal:-According to hospital procedure for electrical and electronic equipment. • Humidifier compatibility:- F& P 950 system only. • Expected service life:-15000 hours of use3 or 7 years1,2,3 whichever is earlier. • Classification:-AU IIA,NZ lla, EU lla. • Country of origin:- New Zealand. PACK OF 01

55 Expiratory heater wire adopted 950x00 • Width:-135mm • Height:-205mm • Depth:-15mm • Weight:-38.25g • Quantity per pack:-1 each • Disposal:-According to hospital procedure for electrical and electronic equipment. • Humidifier compatibility:- F& P 950 system only. • Expected service life:-7 Years1 • CLASSIFICATION:-AU I; NZ; EU I • Country of origin:- China. PACK OF 01

56 Powercode india plug 950x05 F & P950 Power cord , India Plug. PACK OF 01

57 Dual Heated Cpap circuit 950N60 • Neonatal bubble cpap dual heated circuit kit • Contents:- • Chamber • Expiratory limb • Inspiratory limb • Adapters • Bubble cpap • Generator • Pressure manifold • Weight 7.2 kg (pack of 10 including Box.) • Circuit should be dual heated with length of inspiratory tube of 1.75 and expiratory tubing in 1.6m • Should have a resistance of flow of 0.08 ± 0.03 cmH20 • Should have a compliance of 0.61± 0.06 mL/cmH20 • Should be only compatible with the Servo Controlled Heated Device for Ventilator/ BCPAP • Duration of use should be 14 days • Expiratory tubing should have a diffusing membrane to prevent excess rainout • Inspiratory limb should have provision of a thermal adaptor which ensures optimum • heating of the inspiratory limb PACK OF 10

58 Dual Heated Ventie Circuit 950N81 • Adult ventilator dual heated circuit kit (with filter) • Contents:- - Chamber - Expiratory limb - Dryline - Filter - Adapters • Weight 6.3 kg (pack of 10 including Box.) • Circuit should be dual heated with length of inspiratory tube of 1.75 and expiratory tubing in 1.6m • Should have a resistance of flow of 0.08 ± 0.03 cmH20 • Should have a compliance of 0.61± 0.06 mL/cmH20 • Should be only compatible with the Servo Controlled Heated Device for Ventilator/ BCPAP • Duration of use should be 14 days • Expiratory tubing should have a diffusing membrane to prevent excess rainout • Inspiratory limb should have provision of a thermal adaptor which ensures optimum heating of the inspiratory limb PACK OF 10

59 Adult bi-level /cpap heated circuit kit 950A60 • Adult bi-level/cpap heated circuit kit • Contents:- - Chamber - Inspiratory limb - Dryline - Pressure line - Adapters • Weight 5.0 kg (pack of 10 including Box.) PACK OF 10

60 Adult ventilator dual heated circuit kit(with filter) 950A81 • Adult ventilator dual heated circuit kit(with filter) • Contents:- - Chamber - Inspiratory limb - Expiratory limb - Dryline - Filter - Adapters • Weight 6.3 kg (pack of 10 including Box.) PACK OF 10

61 NEONATAL OPTIFLOW JUNIOR HEATED CIRCUIT KIT(950N40) *NEONATAL OPTIFLOW JUNIOR HEATED CIRCUIT KIT *CONTENTS:-- -Chamber - Inspiratory limb -Adapters -Pressure manifold • Weight 3.9 kg (pack of 10 including Box.) PACK OF 10

62 ADULT OPTIFLOW HEATED CIRCUIT KIT(950A40) ADULT OPTIFLOW HEATED CIRCUIT KIT CONTENTS:-- -Chamber -Inspiratory limb -Dryline -Inspiratory limb *Weight 4.5 kg (pack of 10 including Box.) PACK OF 10

63 CHAMBER MR290 VX *Suitable for all MR-series humidifiers *Automatically refills *Dual-float mechanism for added safety to prevent the chamber overfilling *Consistent compressible volume allows for consistent delivery of the prescribed waveform PACK OF 10

64 Neonatal Circuit (SLE5000) + MR290 chamber Dual Heated RT 268 RT268 Evaqua 2 Infant Ventilator Circuit is a specialized, dual-heated, disposable breathing circuit designed for use with SLE5000 series ventilators, incorporating Evaqua 2 technology to minimize condensation in the expiratory limb. (box of 10) Pack of 10

65 DISINFECTION FILTER(900PT601) *Used during the disinfection process to ensure the device is safe for use on a new patient.filter is used in conjunction with the AIRVO 2's disinfection procedure to ensure the airpath is sanitary PACK OF 01

66 Circuit Kit Adult + MR290 chamber Inspiratory Heated ONLY. (RT206) Dual Limb Adult Breathing Circuit Kit with Expiratory Water-trap and Pressure Line, designed for use with the F&P MR850 Respiratory Humidifier. It is a high-performance, single-use circuit designed for adult mechanical ventilation PACK OF 10

67 VISAIRO MASK isairo is a hospital-grade, bridge-free, full-face mask for non-invasive ventilation (NIV), designed to eliminate nasal bridge pressure while maximizing comfort and visibility. It features Dynamic Support Technology (floating seal/stability wings), TubeFit zones for nasogastric/orogastric tubes, and three sizes (A, B, C) with vented/non-vented options (RT075–RT077).*Under-nose full-face mask, designed to fit under the bridge of the nose to prevent skin breakdown.* Dynamic Support Technology combining a floating silicone seal with stability wings.*Available in three, color-coded, size-specific, and anatomically designed sizes: A, B, and C.*RT075: Non-vented (for single-limb circuit with exhalation port or dual-limb).*RT076: Standard (non-vented, or with non-vented elbow).*RT077: Vented (for single-limb circuit). PACK OF 10

68 HIGH FLOW NASAL CANNULA DEVICE AIRVO 3 • It should have inbuilt flow generator and capable of delivering wide range of flow from 2 – 70 LPM. • It should have single mode of operation for neonatal, pediatric and adult patients. • It should have inbuilt Air/O2 blending and FiO2 monitoring, facility to deliver wide range of oxygen concentration from 21% to 100% with suitable menu options. • It should be able to display real time parameters and 24 hours trend data to monitor patient progress. • It should have inbuilt air source without need of external compressor. • It should have integrated heated humidifier. • It should have large, bright and touch screen color display to monitor humidity, flow, FiO2 and error alarms. • It should have visual and audible alarm indications for the errors with error codes. • It should have audible power failure alarm system. • The expected auditory alarm range should be sound pressure level >40 dBA @ 1m, audio pause duration should be 120 seconds. • It should have continuous mode of operation and should have two options for reprocessing for fast turnaround time. • Maximum surface temperature of applied parts should be 44˚C. • It should have operational ambient temperature 18 – 28˚C. • It should have maximum delivered dewpoint temperature of respiratory gas of 43˚C. • It should have target humidity range between 31 – 37˚C. • The humidity should be > 33 mg/L at 37˚C target humidity, 10 – 60 LPM target flow and >12mg/L for all other settings. • It should have dual pressure oxygen port. • It should have dual input manifold to ensure smooth transition to portable oxygen for patient transfer. • It should be supplied with all the necessary compatible accessories like hose pipes and connectors. • It should have integrated battery backup with Lithium-Ion battery with output power of 80 W. The shelf life of the battery should be minimum of 3 years. • Maximum time to recharge the battery should be 6 hours. • Integrated battery should facilitate 40 minutes of transport time, enabling patient mobilization. • Storage and transport ambient temperature should be between 10 – 50˚C. Humidity should be 10 – 95% relative humidity. • The machine should come with 2 years of replacement warranty. • Letter of Authorization from Original Equipment Manufacturer is mandatory. • The machine should be supplied with pole stand, storage basket, oxygen bottle holder, dual input manifold, oxygen hose, water bag and flowmeter. • It should be supplied with 10 units of disposable circuits with humidifier chamber compatible with 22mm vibrating mesh nebulizers. • The disposable circuits should be of similar make as the HFNC machine. • The disposable circuit should have inbuilt heating along with the bore of the circuit which should assist in reduction of condensation. • The circuit should effectively deliver nebulized blended gases. • The disposable circuit should be suitable for use with all interfaces to fit wide range of patients from 2 – 70 LPM. PACK OF 01

69 HIGH FLOW NASAL CANNULA DEVICE --INFANT, PAEDIATRIC AND ADULT- AIRVO 2 1. The device should have integrated flow generator to deliver flows from 2 to 25 litres in junior mode and upto 60 lpm in adult mode. 2. Integrated Air/oxygen blending and Fio2 monitoring with facility to deliver wide range of oxygen concentrations from 21 to 100 %. 3. The oxygen cell should not need infield calibration. . 4. Clinician menu for setting range of Fio2 and flow settings. 5. Inbuilt heated humidifier to deliver warm and humid gases to airway. The humidification chamber should have dual float with auto feed system. 6. Display to monitor temperature of humidified gas, flow rate and fio2 7. Visual and audible alarm indication for : a. Tubes disconnect Leaks, tube blockages, and water out and hardware fault with error codes. Audible power failure alarm. 8. The device should have thermal disinfection mode to minimize contamination. Heated tube for sterilization of the device should be provided with the device. 9. Device should not require servicing and should have 2 years manufacturer warranty. 10. Accessories to be supplied with the system: • Patient breathing tube with integrated heating coil and flow/temperature sensor. • Soft, flexible anatomically contoured nasal cannula. The cannula should be available in different sizes suitable for infant and paediatric application. It should have hydrocolloid adhesive on Velcro to secure on skin. This should be easily replacable. • Air filter – 2 Nos • Disinfection kit – 1 No • Oxygen inlet extension tube- 1 No • Mounting tray and pole with castors & IV hook • The device should be supplied with oxygen flowmeter pole mount for oxygen flow up to 25 liters. 9) Supply frequency: 50/60 Hz, Supply voltage: 220-240 v 10) Sound pressure level 45dbA@1m 11) Oxygen analyzer accuracy +-10 % (within range of 25-80 % Fio2) • The unit should be compliance with international standards. IEC 60601 and ISO 13485 quality standard 11. Certification: US FDA and European CE approved 12. Compliant with international standards. IEC 60601 and ISO 13485 quality 13. Suitable for use in ICU, HDU, recovery, wards and emergency department. 14. We need separate rates for consumables which is used in this machine like circuit, cannula, filters, as per applicable sizes. 15. Authority letter of OEM. PACK OF 01

70 Temperature Probe MR869  Temperature Probe  Airways Temperature and flow  For use with 1.5mtr circuit  With right angle connector MR850  US FDA and CE approved Pack of 1

71 Electrical Adaptor 900MR805  Electrical Adaptor  Dual Heated  RT Circuit  US FDA and CE approved Pack of 1