Supply And Installation Of Picu / Nicu Equipments For Igh Kavaratti Supply , Installation , Commissioning , Provide 3 Years Comprehensive Warranty And 5 Years Camc After Expiry Of Warranty Period For The Picu / Nicu Equipments For Igh Kavaratti-1 Syringe Pump Ntechnical Specifications N1. Should Be Easy To Use And Nurse Friendly 2 2. Should Have Automatic Syringe Size And Model Detection 3 3. Should Have Large Format Lcd / Tft Display. 4 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 – 60 Ml / Hr For 10Ml Syringe. 5 5. Syringe Range From 20-50 / 60 Ml. 6 6. Should Have A Flow Rate Accuracy Of ±2% 7 7. Should Have A Bolus Rate Up To 1000Ml / Hr For 50 Ml Syringe. 8 8. Should Have Automatic And Manual Bolus. 9 9. Should Have At Least 3 Levels Of Programmable Occlusion Pressure. 10 10. Should Have Automatic Bolus Reduction System To Avoid Accidental Bolus Delivery Afterocclusion Incident. 11 11. Should Have A Rechargeable Battery With Back Up Time Of Minimum 3 Hours. 12 12. Pump Must Trigger Following Alarms With Visual Indication:- Ni. Occlusion Pressure Alarm Nii. Kvo Or 3 Min Pre- Alarm Niii. Syringe Empty And Volume Infused Alarm Niv. Internal Malfunction And Battery Charge Low Alarm Nv. Syringe Disengaged And Incorrectly Placed Alarm Nvi. Alarm Loudness Control. Nvii. No Mains Nviii. Line Disconnected ( Rapid Pressure Drop ) . N 13 13. Should Work With Input 200 To 240Vac 50 Hz Supply. 14 14. Should Have Safety Certificate From A Competent Authority Ce / Fda ( Us ) / Stqc Cbcertificate / 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 15 Infusion Pump Nspecification N1. The Syringe Pump Should Be Programmable, User Friendly, Safe To Use And Should Have Battery Backup And Comprehensive Alarm System. 16 2. Must Work On Commonly Available Standard 5Ml / 10Ml / 20Ml / 50Ml / 60 Ml Syringes With Accuracy Of Minimum Of + / -2% Or Better, With Automatic Syringe Size Recognition. 17 3. Manufacturer Should Be Iso And European Ce Certified For Quality Standards. 18 4. Flow Rate Programmable From 0.1 To 1000 Ml / Hr Or More In Steps Of 0.1 Ml / Hr With User Selectable Flow Set Rate Option. Save Last Infusion Rate Even When The Ac Power Is Switched Off. 19 5. Bolus Rate Should Be Programmable To 40 To 1000 Ml / Hr Or More With Infused Volume Display And One Key Press Bolus, Auto Bolus As A Advance Feature With Programmable Bolous Rate. 20 6. Display Of Drug Directory Of More Than 50 Drugs, Customized And Adjustable. 21 7. Key Board Locking System For Patient Safety. 22 8. Keep Vein Open ( Kvo ) Must Be Available 1.0 Ml / Hr Or Set Rate If Lower Than 1.0 Ml. User Should Have Choice To Disable Kvo Whenever Desired. 23 9. Selectable Occlusion Pressure Trigger Levels Selectable From 300 / 500 / 900 Mmhg. 24 10. Automatic Detection Of Syringe Size & Proper Fixing. Must Provide Alarm For Wrong Loading Of Syringe Such As Flanges Out Of Slot; Disengaged Plunger, Unsecured Barrel Etc. 25 11. Manual Pusher With Plunger Protection Guard. 26 12. Anti-Bolus System To Reduce Pressure On Sudden Release Of Occlusion. 27 13. Should Have Comprehensive Alarm Package Including: Occlusion Limit Exceed Alarm. Near End Of Infusion Pre-Alarm & Alarm, Volume Limit Prealarm& Alarm, Kvo Rate Flow, Low Battery Prealarm And Alarm, Ac Power Failure, Drive Disengaged And Preventive Maintenance. 28 14. Rechargeable Battery Having At Least 8 Hours Backup For About 5Ml / Hr Flow Rate With 50Ml Syringes. Larger Battery Life And Indication Of Residual Life Will Be Preferred. 29 15. Docking Station For Two Or Four Pumps As Per Requirement So As To Enable To Power Up To 2-4 Pumps With One Power Cord When Mounted On Iv Pole. 30 16. The Unit Shall Be Capable Of Stored And Operating Continuously In Ambient Temperature Of 10 - 50Deg C And Relative Humidity Of 15- 90% . 31 17. Power Input To Be 220-240Vac, 50Hz. 32 18. User Manual And Service Manual In English. 33 Double Surface Led Phototherapy Nspecification N1. Should Last For At Least 30, 000 Hours 34 2. Should Be Made Of Easily Cleanable Material 35 3. Minimum Irradiance Should Be 20 Μw / Cm2 / Nm At 45Cm Distance Between Bed And Light Unit 36 4. Wave Length Should Be 450-460 Nm And Should Be Free From Uv And Ir Radiation 37 5. Should Have Visual And Audible Alarms For The Following - N• Internal Temperature >550C N• If Cooling Fan Fails N• If Led Current Increases Or Decrease N• If Led Volt Increases Or Decreases 38 6. Cooling Fan To Be Provided To Dissipate The Heat Created By Led 39 7. Should Be Compact To Use Along With The Radiant Warmer And Should Have Tilting Facility So That Unit Is Not Coming Directly Under Warmer 40 8. Smooth Height Adjustment Mechanism & Adjustable Height 41 9. Peak Spectral Irradiance: At Least 30 Μw / Cm² / Nm At 30 Cm Distance And 50 Μw / Cm² / Nm At 20 Cm Distance ( As Measured With Minolta-Airshields Or Olympic Flux Meter ) 42 10. It Should Be Possible To Increase Or Decrease The Irradiance By A Switch Without Changing The Distance To The Baby 43 11. Large Effective Surface Area: Mean Spectral Irradiance Of At Least 20 Μw / Cm² / Nm Over An Area Of 25Cm By 50Cm At 30Cm Distance 44 12. Emissions Spectrum: Blue Light With A Peak Wavelength Between 440 And 470 Nm 45 13. The Source Of Lamps ( Manufacturer ) Should Be Identified And Acertificate Of The Emission Spectrum From A Government / Research Laboratory Should Be Provided. 46 14. Quality Control: Device Is Produced By Manufacturer With Iso 9001 Certification ( Certificates To Be Submitted ) 47 15. Electrical: Device Is Compatible With 220 -240 V50 / 60 Hz Power Input 48 16. Durability: Leds Are Protected By Suitable Cover Made Of Fire-Resistant Transparent Material 49 17. Digital Lamp Time Counter 50 18. Digital Treatment Time Counter 51 19. Leds Are Protected By Suitable Cover Made Of Fire-Resistant Transparent Material 52 20. Sturdy Mobile Stand 53 21. At Least 2-Inch Sturdy Castors, At Least 2 Should Have Breaks 54 22. Height Of Stand’S Base Must Be Less Than 8Cm To Fit Under Radiant Warmers / Incubators And Baby Cots 55 23. Height Adjustable From 1.20M To 1.50 M ( Measured From Bottom Surface Of Enclosure To Ground ) Ni. Light Enclosure Must Be Tiltable From Horizontal To At Least 30 Degrees Nii. Tiltable From Horizontal To At Least 30 Degrees 56 24. The Base Of The Unit Should Be Such That It Will Go Beneath Any Incubator / Bed / Trolley With Minimum Of 100 Mm Floor Clearance. 57 25. 1 Spare Set Of Fuses Per Machine N1. All The Material / Equipment Should Be European Ce & Us Fda. N2. All The Electronic Equipment’S Should Comply With Electrical Safety Conforms To Standards For Electrical Safety Iec 60601-1. N3. All The Equipment’S Power Input Should Be 220- 240V Ac, 50Hz Fitted With Indian Plug. 58 Multipara Monitor With Paediatric And Neonatal Bp Cuff Nspecification Ngeneral: N• Parameters – Ecg, Heart Rate, Respiratory Rate, Spo2, Nibp, Dual Ibp, Etco2, Dual Temperature. N• Should Be Modular And Capable Of Being Connected To A Central Station. N N N N N N 59 • The Equipment Should Come With All Standard Accessories Nrequired To Run All Parameters. 60 • Waveform Display: At Least 12 Channels At A Time, User Selectable. 61 • Digital Display: Heart Rate, Respiratory Rate, Oxygen Saturation, N Temperature, Blood Pressure ( Systolic, Diastolic, Mean ) . 62 • System Should Be Compatible With His. 63 • System Should Be Us Fda & European Ce Approved For Nquality Assurance. 64 • Monitor Must Be Able To Connect To Central Monitoring Station And Nshould Use Single Network For All Kind Of Networking With The Central Station Or Other Hospital Information System ( His ) . It Should Have Dual Display, One For Continuous Display Of All Beds And Other For Trend Review, Full Disclosure Etc. 65 Individual Monitors: N• Wall-Mountable And Pivotable. N* Medical Grade, Tft Flast Screen, , Slim Size, At Least 19 Display N• Flexible Display Mode For Various Monitoring Needs. N• Should Be Knob Control And Touch Screen. N• Viewing Angle At Least 90O. N• Bigger Font Of Numeric Should Also Be Available. N• Should Have Standby Mode For Temporary Leaving Of Patients. N• Adjustable Contrast And Brightness. 66 Should Have Facility To Record Data For Individual Patients Identifiable By Their Name And Hospital Registration Number Nthe Following Modules Complete With Their Accessories For Each Monitor: N• Heart Rate N• Ecg N• Respiration N• Oxygen Saturation N• Temperature: 2 Ports N• Non-Invasive Blood Pressure N• Invasive Blood Pressure 2 Ports N• Etco2 N 67 The Following Modules Are Also Required In The Quantity Mentioned Nparameters Monitored: Cost Of Following Modules Should Be Quoted Separately. N• Eeg – 2 N• Nmt – 1 N• Minimal Invasive Cardiac Output Monitor – 2 N• Bis - 1 N 68 3. Heart Rate / Ecg: N• 10-Lead Selectable Ecg N• Built In Arrhythmia Monitoring In All Leads N• Inbuilt St Segment Analysis And Arrhythmia Detection Facility N• Display Of 2 Ecg Leads Simultaneously At A Time N• Heart Rate Range 20-250 Bpm N• Accuracy ± 5 Bpm N• Display Sweep Speeds 12.5, 25 Mm / Sec ( User Adjustable ) N• Averaging Time: User Selectable Up To 8 Seconds N• Ecg Amplitude User Adjustable N• Defibrillator Protected N N N 69 4. Respiratory Rate N• Measured By Transthoracic Impedance Using The Same Ecg Lead N• Range 0 To 150 Breaths / Min N• Accuracy ± 2 Bpm N• Display Sweep Speeds 6.25, 12.5 & 25 Mm / Sec ( User Adjustable ) N• Averaging Time: User Selectable Up To 8 Seconds N• User Selectable Apnea Alarm Time N N 70 5. Oxygen Saturation N• Masimo-Set / Fast Technology To Take Care Of Low Perfusion States And Motion Artifacts N• Dual Wavelength Led Pulse Oximetry N• Range 1 To100% N• Spo2 Accuracy : ± 2 % ( 70-100% Range ) N• Averaging Time: User Selectable Up To 8 Seconds N• Plethysmographic Waveform Display N• System Must Display Perfusion Index ( Pi % ) From Spo2 As An Indication Of Pulse Strength At The Sensor Site. N 71 6. Temperature N• 2-Channels N• Continuous Digital Display Of Two Site Temperatures N• Range: 25-50 Degree Celsius N• Resolution: ± 0.1 Degree Celsius N• Accuracy: + 0.1 Degree Celsius N• Should Provide Skin Temperature Probe And Rectal Temperature Probe For Every Monitor. N N 72 7. Noninvasive Blood Pressure: N• Capable Of Measuring Blood Pressure Including In Neonates Weighing 500 G N• Microprocessor Software With Unit In Mmhg N• Oscillometric Technique N• Manual, Auto And Time Limited Stat Modes N• User Selectable Automatic Time Intervals N• Display Systolic, Diastolic And Mean Bp N• Blood Pressure Range Nsystolic : 30-250 Mm Hg Ndiastolic : 10-200 Mm Hg Nmean: 20 – 100 Mmhg N• Pulse Rate Range : 20-250 Bpm N• Cuff : Auto Deflate With Over Pressure Protection N• Should Automatically Establish Zero Reference After Each Reading N N 73 8. Invasive Blood Pressure N• At Least 2 Channels N• Compatible With Reusable And Disposable Pressure Transducers N• Transducer Should Allow Continuous Infusion Into The Artery Through An Infusion Pump While Pressure Is Simultaneously Displayed N• Input Through Pressure Transducer That Functions Through A Fluid Filled Catheter System 74 • Unit: Mmhg N• Should Allow Continuous Fluid Infusion Into The Artery / Vein Through An Infusion Pump Without Any Volume Limitation N• Compatible With Arterial Bp, Cvp And Intracranial Pressure Monitoring Catheters With User Selectable Display Names 75 • Range 0-350 Mmhg N• Display Resolution: ±1 Mmhg N• Accuracy ± 1Mmhg N• Digital Waveform Display N• User Selectable Pressure Channel Display 76 • Should Be Compatible With Icp Monitoring System N• Name Of Manufacturer Of Compatible Icp Monitoring System Should Be Provided With Documentary Evidence. N• Monitor Must Measure Dynamic Preload Parameters Such As Pulse Pressure Variation ( Ppv ) And Systolic Pressure Variation ( Spv ) From Arterial Waveform And Display On Main Screen. 77 9. Etco2 N• Should Provide Mainstream Modules-2Nos And Microstream – 2 Nos. N• Warm Up Time: Capnogram Displayed In Less Than 15 Sec N• Measurement Method: Infrared Spectrum N• Unit: %, Mmhg, Kpa N• Co2 Accuracy: + / - 2.0 Mmhg N• Measurement Range: 0-150 Mmhg N• Resolution: 1 Mmhg N• Resp Rate Accuracy + / - 1 Rpm N• Range Of Resp Rate Measurement: 0-150 / Min N• Should Also Be Able To Monitor Etco2 By Non-Invasive ( Nasal ) Way From The Same Module. N 78 10. Eeg N• Eeg Module Should Be Interchangeable With Any Of The Monitors Input: 6 Lead N• Sensitivity: 20, 50, 100, 250 / Μv / Cm N• Display: Left Or Right Sided Waveform N• Small, Cup Type Eeg Electrodes And Lead Set Kit Suitable For Neonatal Use With A Low Impedance N 79 11. User Selectable Alarms N• High And Low Heart Rate N• High And Low Respiratory Rate N• Apnea With Adjustable Time 5-20 Seconds N• High And Low Saturation N• High And Low Sbp N• High And Low Dbp N• High And Low Map N• Probe Failure N• Poor Signal N• Power Failure N• Audio & Visual Alarms With Message With Separate Alarm Indicator With 3600Viewing. N N 80 12. Trends N• Memory Storage : At Least 72 Hours N• Data Display Interval : Not More Than 20 Sec N• Display Range : Last ½ Hour To 72 Hours N• Graphical And Tabular Format Of Display Of Variables N• Full Waveform Disclosure Of 24 Hrs. N 81 13. Power N• 220 / 240 V 50 / 60 Hz Ac N• Rechargeable Internal / External Battery With A Backup Of At Least 1 Hr N 82 14. Manuals: One Set Of Operator & Service Manuals With Each Monitor N15. Comprehensive Warranty Period: 5 Years And Cmc For 5 Years After Warranty N16. Availability Of Spares For At Least 10 Years After Date Of Installation N 83 The Following Quantities Are To Be Supplied For Every Monitor With The Initial Order: Ecg / Respiration N• Ecg Patient Cable : 2 N• Reusable Ecg Lead Wires Set : 2 Sets N 84 Oxygen Saturation N• Patient Extension Cables: 2 N• Reusable Neonatal Wrap Around Probes: 4 N• Reusable Pediatric Clip / Finger Probes: 4 N 85 Temperature N• Reusable Surface ( Skin ) Temperature Probes: 2 N• Reusable Rectal Temperature Probes: 2 N 86 Nibp N• Patient Extension Cable – 2 N• Disposable Nibp Cuffs Suitable For Neonates, Children And Adults ( <1000G, 1000-2000G, >2000G, Pediatric, Adolescent And Adult ) : 5 No Of Each Size. N 87 Ibp N• Transducer Connecting Cables: 2 N• Reusable Pressure Transducer: 5 N• Disposable Pressure Dome Kit With Neonatal Flush Device: 10 N• Quotation Must Include A Compliance Statement And In Addition, Each Of The Above Points Is Marked In The Technical Brochure. Points Not Covered In The Brochure Must Be Specifically Addressed In A Separate Certificate. N 88 Manuals: N• One Set Of Operator & Service Manuals With Each Monitor N• Should Be Able To Provide Training Of All Healthcare Personnel During First 1 Month Of Installation In The Group Of 5 Trainees Per Session. N• Fda ( Usa ) And Ce Certificate Must Be Enclosed. N• Onsite Physical Demonstration Of The Machine With All Standard Actual Accessories Of The Same Make Which The Firm Intends To Supply Will Be Mandatory If Demanded By The Technical Committee. N• The Machine With All The Accessories Has To Be Left In The Unit For Demonstration On Real Patients For At Least 1 Month. N• Prices Of The Above Consumable Accessories Should Be Quoted Separately, Which Will Be Fixed For The Duration Of Comprehensive Warranty And Camc. N N 89 5. Pulse Oximeter Nspecification N1. Desktop Sturdy Compact Model Which Is Light Weight N2. Resistant To Motion Artifact N3. Able To Reliably Pick Up Signal In Low Perfusion States N4. Should Have Clinically Proven Track Record To Work During Motion And Very Low Perfusion Conditions N5. Compatible With Reusable And Disposable Probes 90 6. Device Should Be Able To Continuous Monitor The Nfollowing Parameters Non-Invasively: Na ) Oxygen Saturation Nb ) Pulse Rate Nc ) Perfusion Index Nd ) Pleth Variability Index Ne ) Total Hemoglobin Nf ) Carboxyhemoglobin Ng ) Methemoglobin Nh ) Oxygen Content N 91 7. Oxygen Saturation Na ) Display Range 0 To 100 % Nb ) Resolution 1% Nc ) Accuracy + 3 At 70-100% Range Nd ) Alarm Range 1% To 99% N 92 8. Pulse Rate Na ) Display Range 25 Bpm To 240 Bpm Nb ) Resolution 1 Beats Per Minute Nc ) Accuracy ± 3 Bpm Nd ) Alarm Range 30 Bpm To 235 Bpm N 93 9. Perfusion Index Na ) Display Range 0.02% To 20% Nb ) Alarm Range 0.03% To 19% N 94 10. Pleth Variability Index Na ) Display Range 0% To 100% Nb ) Alarm Range 1% To 99% N 95 11. Total Hemoglobin Na ) Display Range 0 G / Dl To 25.0 G / Dl Nb ) Resolution 0.1 G / Dl Nc ) Accuracy 8 G / Dl To 17 G / Dl ±1 G / Dl Nd ) Alarm Range 1.0 G / Dl To 24.5 G / Dl N 96 12. Carboxy Hemoglobin Na ) Display Range 0% To 99% Nb ) Resolution 1% Nc ) Accuracy 1% To 40% ± 3% Nd ) Alarm Range 1% To 98% N 97 13. Methemoglobin Na ) Display Range 0% To 99.9% Nb ) Resolution 0.1% Nc ) Accuracy 1% To 15% ± 1% Nd ) Alarm Range 0.1% To 99.5% N 98 14. Oxygen Content Na ) Display Range 0 Ml To 35 Ml 99 15. Should Be Able To Measure Parameters Reliably Nin Patient < 1Kg Of Weight 100 16. Should Be Defibrillator Proof 101 17. Display Na. Large Bright Lcd Display With Contrast Adjustability Nb. Readable From At Least 3 Feet Nc. Alarms And Alarm Limits Nd. Status Of Battery Charging, Sensor Off N 102 18. Alarms Na. Type Of Alarm Audible And Visual Nb. Alarm Volume Adjustable Nc. System Alarms Probe Failure, System Failure, Low Battery N 103 19. Alarm Override Facility Should Be Present 104 20. Trends Na. Memory At Least 48 Hours With 2 Sec Resolution Nb. Data Interval 20 Sec Nc. Display 2-24 Hours Nd. Type Of Display Graphical & Tabular Display N 105 21. Power Na. 220 / 240 V Ac, 50 / 60 Hz Nb. Rechargeable Internal Battery Nc. Battery Back-Up At Least 3 Hours Nd. Automatic Switch From Mains To Battery In Case Of Power Failure N 106 22. Rs 232C Interface For Data Communication 107 23. Should Have Provisions For Wireless And Blue Tooth Connectivity 108 24. Accessories Ni. Patient Extension Cables -2 With Each Monitor Nii. Reusable Flexible Neonatal Multi-Site Probes-4 With Each Monitor N 109 25. Operator Manual To Be Provided. N26. Should Have Local Service Facility And Should Have The Necessary Equipments To Ncarry Out Preventive Maintenance Test N 110 27. Onsite Physical Demonstration And Training Of The Equipment To N All The End Users With All The Requested Facilities Will Be Mandatory N28. Availability Of Spares For At Least 7 Years After Date Of Installation N 111 29. Items Covered Under Warranty / Cmc Na ) Prices Of Consumables Should Be Quoted Separately And Frozen For The Period Including Warranty And Cmc Period 112 30. Standards, Safety And Training Na ) Should Be Us Fda And European Ce Approved Product And Certificate Of The Offered Model Must Be Submitted With The Bid Documents Nb ) Manufacturer Should Be Iso Certified For Quality Standards Electrical Safety Conforms To Standards For Electrical Safety Iec 60601-1 ( Or Equivalent International / National Standard ) General Requirement For Electrical Safety Of Medical Equipment Should Have Local Service Facility Nc ) The Service Provider Should Have The Necessary Equipments Recommended By The Manufacturer To Carry Out Preventive Maintenance Test As Per Guidelines Provided In The Service / Maintenance Manual N 113 31. Environmental Factors Na ) Shall Meet Iec-60601-1-2:2001 ( Or Equivalent Bis ) General Requirements Of Safety For Electromagnetic Compatibility Or Should Comply With 89 / 366 / Eec; Emc-Directive. Nb ) The Unit Shall Be Capable Of Being Stored Continuously In Ambient Temperature Of 0-50Deg C And Relative Humidity Of 15-90% Nc ) The Unit Shall Be Capable Of Operating Continuously In Ambient Temperature Of 20-40 Deg C And Relative Humidity Of 15-90% N 114 32. Onsite Physical Demonstration / Training Of The Equipment To N All The End Users With All The Requested Facilities Will Be Mandatory 115 33. Documentation Na ) User / Technical / Maintenance Manuals To Be Supplied In English Nb ) Certificate Of Calibration And Inspection From Factory Nc ) List Of Important Spares And Accessories With Their Part Number And Costing Out. N 116 Neonatal Bubble Cpap With Oxygen Blender Nspecification N1. The Instrument Should Be Suitable To Provide Respiratory Care In Both Term And Preterm Neonates Weighing 500 G To 5000 G. 117 2. Light Weight, Portable And Sturdy. N3. Stainless Steel Stand - Corrosion-Free, Dust Resistant, Stainless Steel N4. Cpap Pressure With Oscillations Should Be Generated By Creating Resistance In Water Column And Bubbling Of Exhaled Gas In The Water Column. N5. The System Should Be Suitable For Both Cpap And High Flow Nasal Cannula Therapy. N 118 6. Cpap Generator N• Pressure: 3 To 12 Cm H2o N• Has Detachable Overflow Container N• Delivers Intended Pressure Constantly And Accurately ( + 1Cm ) N• Easy To Clean / Sterilize N• Gradations On The Sliding Rod Should Be Easily Visible From A Distance Of 4 Feet. N 119 7. Safety Features N• Limiting The Delivered Pressure In The Event Of An Occlusion N• A Stand Or Arm Support For Holding The Circuit In Support N 120 8. Humidifier Nit Should Be Servo Controlled Heated Humidifier With Following Features: N• Temperature And Flow Sensor With Feedback Mechanism. N• Monitoring Temperature Of Gas At Chamber End And Near Patient End Additionally Temperature Of Airway, Chamber And Heater Plate. N• Display For Temperature Of Saturated Gas. N• Modes: Intubated And Mask Mode. N 121 Alarms N• High Temperature And Low Temperature. N• Water Out Alarm / Pop Off Pressure Adjustment. N• Heater Adaptor Faulty / Disconnect. N• Temp Cum Probe Faulty / Disconnect. N• Hardware Faults. N• Heater Wire With Adapter To Be Provided N 122 9. Delivery System Nthe Patient Heating Circuit Should Have Integrated Heated Coil For Uniform Heating. Nthe Delivery System Should Have Maximum Input Flow- 15L / Min And Maximum Mean Cpap- 15Cmh20. N 123 Humidification Chamber Should Be Auto Feed With Dual Float System Nchamber Compressible Volume 260- 300 Ml Ncompliance Of Chamber 0.4Ml / Cm / H20 Nmax Peak Flow Should Be 180 L / Min. N 124 10. Cpap Bubble Generator Should Have Adjustable Probe For Pressure Settings 3-10 Cm Of H2o.It Should Have Detachable Overflow Container To Maintain Constant Water Level. Volume For Generator ~ 500 Ml. 125 11. Air-Oxygen Blender N• The Instrument Should Be Suitable To Provide Air-Oxygen Mixture To Neonates N• Should Be Compatible With Bubble Cpap System N• Fio2 Concentration Will Be Adjustable ( 21-100% ) And Accurate N• Should Be High & Low Flow ( Flow Rate Of 3-30 L / M ) , Accuracy Of + / - 3 Percentage And Bleed Flow Of 2.5-3.5 N• Should Have Stand & Pole Assembly To Incorporate Air & O2 Blender With Flow Meter N• Should Be Supplied With Connecting Tubes And Adapter To Be Attached With Oxygen And Compressed Air Source N 126 12. 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. 127 13. Interface N• Nasal Prongs / Masks Of Silicon Of At Least Five Different Sizes Useful For Babies Weighing Between 750-1250G, 1250-1750G, 1750-2000G, 2000-2500G. Where The Resistance To Flow At Pressure Port Of Nasal Tubing Should Be 0.4 Cm H20, 0.6 Cmh20 Or 0.2 Cm / H20. 128 • Flexible Nasal Tubing With Glider Technology From Block And Fixing Guide With Sizes Ranging From 50Mm To 100Mm Where Resistance To Flow Should Be 0.49 Cm / H20, 0.53Cm / H20, 0.55 Cm / H20 Respectively Flow Of 6 Lit / Min. N• Infant Caps Of Following Sizes: 17-22, 22-25, 25-29, 29-36 Cm Circumference. N• Nasal Cannula Of Preterm And Term Sizes. Cannula Should Be Kink Proof And Have Hydrocolloid Based Adhesive To Secure On Skin And Facilitate Kangaroo Mother Care. N• Nasal Masks Suitable For Preterm And Term Babies. N• Nasal Masks Should Be Interchangeable To Nasal Prongs. N• The Mask Should Be Soft And Anatomically Shaped. N 129 14. It Should Have Mobile Trolley To Fix Humidifier, Cpap Generator And Monitor And Pole With Castors & Iv Hook And Mounting Brackets Gas Supply Lines To Blender. 130 15. Documentation N• User / Technical / Maintenance Manuals To Be Supplied In English N• Certificate Of Calibration And Inspection From Factory N 131 16. General Requirement For Electrical Safety Of Medical Equipment N17. Onsite Physical Demonstration Of The Monitor With All The Requested Modules Will Be Mandatory N18. Should Have Local Service Facility 132 19. The Service Provider Should Have The Necessary Equipment’S Recommended By The Manufacturer For Installation And To Carry Out Preventive Maintenance Test As Per Guidelines Provided In The Service / Maintenance Manual. N 133 20. Patient Circuits Na. Disposable Circuits Should Be Readily Available And Reasonably Priced Nb. A Single Patient Circuit Pack Should Contain All The Necessary Tubing / Connectors Needed To Assemble A Complete Circuit Nc. Should Have All Connections / Connecting Tube With Standard Wall Fittings / Air-Oxygen Outlets Nd. Should Have Heater Wire In Inspiratory Limb Ne. Should Have Water Trap In Expiratory Limb Nf. Should Be Compatible With Available Interfaces Including Nasal Masks N 134 21. The Entire System Including Air Oxygen Blender Should Be Approved By Us Fda Or Its Equivalent National Certifying Authority 135 22. Each Unit To Be Supplied With: N• Disposable Circuits: 25 N• Nasal Interface: 25 N• All Size Nasal Prongs: 10 Sets N• All Size Head Bonnets: 10 Sets N 136 23. Prices Of Above Consumables And Accessories Should Be Quoted Separately In The Financial Bid. N24. Comprehensive Warranty For At Least 5 Years. 137 25. Good After Sales Service With At Least 3-Monthly Visits For Routine Checking And In Between Whenever Called For Troubleshooting. N26. Company Should Ensure The Supply Of Consumables And Accessories For The Period Of Warranty And Cmc. 138 Portable Blood Gas Analyser Nspecification N1. The System Is Required To Analyse Blood Gases In Arterial And Venous Blood At Bedside. N 139 2. It Should Provide The Readings Of Ph, Po2, Pco2, Tco2, Hco3, Base Excess, Sodium, Potassium And Haematocrit. 140 3. The System Should Be Able To Report The Values Accurately In The Range – Ph ( 6.5-8.0 ) , Po2 ( 40-400 Mmhg ) , Pco2 ( 10-100 Mmhg ) , Tco2 ( 5-50 Mmol / L ) , Hco3 ( 5-70 Mmol / L ) , Base Excess ( -25 - +25 Mmol / L ) , Sodium ( 110-170 Mmol / L ) , Potassium ( 2-8Mmol / L ) And Haematocrit ( 20-60% ) . 141 4. The Process Time Should Be < 5 Minutes N5. The System Should Preferably Have Facility For Wireless Transfer Of Reports To The Hospital Information System. 142 6. The System Should Be Supplied Along With Inbuilt Printer. N7. The System Should Be Factory Calibrated. The Supplier Should Perform Quarterly Calibration, To Maintain Accuracy Of The System. 143 8. It Should Have Provision To Be Battery Operated. N9. It Should Be Us Fda / European Ce Certified. N10. It Should Function At Temperature Range 15? To 50?. N N 144 11. Manufacturer Should Have Iso 9001:2008 Certification. N12. Analyzer Should Comply With Ivd Medical Device Directive 98 / 79 / Ec 145 Heated Humidified High Flow Nasal Cannula Therapy Device Nspecification N1. Suitable For Treatment Of Hypoxemic Patients With Respiratory Distress N2. It Should Be Complaint For Use On Patients In Icu, Wards, Emergency Department And Nhome Oxygen Therapy N 146 3. It Should Be Single System For Treating Infants, Paediatric And Adult Patients N4. Inbuilt Flow Generator Capable Of Delivering Wide Range Of Flows:2-25 Litres In Npaediatric Mode And 10-60 Litres In Adult Mode N 147 5. Inbuilt Air / O2 Blending And Fio2 Monitoring, Facility To Deliver Wide Range Of Oxygen Concentration ( Fio2 ) From 21 To 100% N6. It Should Have Inbuilt Air Source Without Need For External Compressor N7. Integrated Heated Humidifier 148 8. Color Display To Monitor Humidity Setting, Flow, Fio2 And Faults N9. Visual And Audible Alarm Indication For: Na. Tubes Disconnect Leaks, Tube Blockages And Water Out And Hardware Fault With Error Codes. Audible Power Failure Alarm N 149 10. Disinfection Mode With Heated Disinfection Tube For Sterilization Of The Device After Patient Use N11. Supplied With Heated Wire Patient Breathing Tube And Nasal Cannula Of Different Sizes N12. Paediatric Nasal Cannula Should Be Made Of Kink Proof Material And Has Adhesive Nwiggle Pads To Stick On Skin To Facilitate Kangaroo Care N 150 13. It Should Be Compatible For Use On Tracheostomy Patients N14. Should Have Safety Certificate From A Competent Authority Ce Issued By A Notified Body Nregistered In The European Commission / Fda ( Us ) / Stqc Cb Certificate / Stqc S Ncertificate Or Valid Detailed Electrical And Functional Safety Test Report From Ertl. Copy Nof The Certificate / Test Report Shall Be Produced Along With The Technical Bid N 151 15. Complaint With International Safety Standards And Regulations. N 152 9.Cash Cart Nspecification N1. Size -940X490x1535 Mm Approx. N2. Trolley With 25 Mm Diameter Ss Tubular Frame N 3. Drawers Maximum Number Possible Of Adequate Size 153 4. Flat Surfaces Should Be Stainless Steel. N5. Two / Three Rows Of Hand Out Bins Of Different Size &Color To Hold Different Sizes Of Ampoules / Vials Of Emergency Medicine. 154 6. Light Weight Plastic Box With Drawers Of Different Sizes And Colors Nto Hold Emergency Medicines, Ambu Bag, Iv Solution , Catheters Etc Separately. N7. Facility To Carry Monitor & Suction Apparatus. N8. Stainless Steel Saline Rod-One. 155 9. Castor Wheels Of 12.5 Cm Diameter With Two Having Locking Arrangement. N10. Pull Out Cardiac Massage Board Above Drawers. N11. Oxygen Cylinder Stand On One Side. N12. All Parts Should Be Epoxy Polyster Coated With 50 Micronethichness Approx. Ebonite Rubber , Pvc And Castor Wheel Etc. N13. Whole Crash Cart Should Be Washable. 156 Radiant Baby Warmer / Neonatal Resuscitation Unit Nspecification N1. Essential Parts Na ) Quartz Based Warming System With Microprocessor Based Controls, Probes & Alarms Nb ) Cart & Bassinet Nc ) Examination Light Nd ) X-Ray Cassette Holder N 157 2. Cart Na ) Should Swivel On 4 Wheels Of At Least 4” Diameter With Foot Operated Brakes On At Least 2 Front Wheels 158 3. Dimensions Na ) Height - 180- 200 Cms Nb ) Width - 65-80 Cms Nc ) Depth - 100-120 Cms Nd ) Working Level - 95-105 Cm N 159 4. Bassinet Na ) Collapsible Transparent Acrylic Side Walls 160 5. Mattress Na ) Width - 70 - 80 Cms Nb ) Length - 90 - 100 Cms Nc ) Thickness - 3-5 Cm Nd ) Material Ni. Soft And Easy To Clean Nii. X-Ray Transparent Niii. Fire Retardant Niv. Allows Air To Pass Through But Does Not Allow Water To Seep In N 161 6. Bassinet Tilt Na ) Should Allow Tilt For Trendelenburg As Well As Reverse Trendelenburg Position 162 7. Warming System Na ) Quartz Based Heating System Encapsulated Heater Tube Placed In A Parabolic Reflector Nb ) Should Have Single Element Quartz Infrared Heater Nc ) Control - Microprocessor Controlled Nd ) Self-Test Function Performed At Power On Ne ) Digital Display Should Show Following Parameters Ni. Set Temperature Nii. Present Temperature Of The Baby Niii. Heater Output Niv. The Temperatures Should Be In Numerical Led Display N 163 F ) Mode - Manual & Skin ( Servo ) Ng ) Manual Mode Ni. Adjustable In Steps From 0 To 100% In Increments Of 10% Nii. Heater Power Should Be Reduced To 50 - 60% After 10-15 Minutes In Manual Mode For Baby Safety N 164 H ) Skin Mode ( Servo Mode ) Ni. Set Point Range - 32 – 38 Degrees C Ni ) Skin Temperature Display Ni. Accuracy - ±0.2 Degrees C Nii. Resolution - 0.1 Degree C Nj ) Temperature Probe- Wire Should Be Easy To Clean And Long Lasting Nk ) No Need Of Temperature Probe Calibration N N 165 8. Alarms Na ) Audiovisual Alarms With A Display Of Text Messages About The Alarms Ni. Probe Failure Nii. Heater Failure Niii. High And Low Baby Temperature ( More Than 0.5 Deg C Difference ) Niv. Power Failure Nv. System Failure Nvi. Silence / Reset Switch Nvii. Should Have Automatic Cut-Off Of Heater At 39°C For Over Temperature Protection N 166 9. Heating Unit - Should Be Swivable For Accommodating X-Ray Unit And N Should Have Self-Lock Facility. 167 10. Examination Light Na ) Illuminance - At Least75 Foot Candles At Mattress Centre N11. Apgar Timer Na ) Timer With Stopwatch Facility Nb ) Reset Facility N 168 12. I.V. Stand Na ) Strong Iv Stand ( S.S ) With Height Adjustable And Facility To Fix Large Number Of Infusion Pumps 169 13. Monitor Shelves - Two In Number N14. Should Have T Piece Resuscitator Inbuild Inside With Standard Recommendation For Neonatal Resuscitation. N15. Should Have Two Drawers N 170 16. X- Ray Cassette Holder Na ) Sliding Holder Located Just Below Undersurface Of Bassinet, With Markings To Help Placement Of Cassette 171 17. Power Consumption - Less Than 1 K.W 172 18. All Metal Parts Of The Equipment Should Be Corrosion Resistant And Epoxy / Powder Coated 173 19. All Consumables Required For Installation And Standardization Of System To Be Given Free Of Cost 174 20. Standards, Safety And Training. Na ) Should Be European Ce Approved Product And Certificate Needs To Be Submitted Along With The Catalogue Nb ) Manufacturer Should Be Iso 13485 Certified For Quality Standards Nc ) Electrical Safety Conforms To Standards For Electrical Safety Iec 60601-1 ( Or Equivalent International / National Standard ) General Requirement For Electrical Safety Of Medical Equipment Nd ) Should Have Type Of Protection Against Electric Shock: Class 1 Ne ) Should Have Degree Of Protection Against Electric Shock: Type B N 175 21. Power Supply And Electrical Specifications Na ) Power Input To Be 220-240Vac, 50Hz Nb ) Suitable Autovoltage Corrector With Spike Protector Should Be Available Nc ) Should Have Overload Protection At 4A Nd ) Should Have Leakage Current <0.5Ma Ne ) Should Have Earth Resistance <0.2 Ohm Nf ) Should Be Low Noise Ng ) Fuse Rating Should Be Ni. For Main Supply: For 230V: 4A & For 110V: 8A Nii. For Examination Lamp: For 230V: 2A & For 110V: 2A N 176 22. Enviornmental Factors Na ) Shall Meet Iec-60601-1-2 :2001 General Requirements Of Safety For Electromagnetic Compatibility Or Should Comply With 89 / 366 / Eec; Emc-Directive Nb ) The Unit Shall Be Capable Of Being Stored Continuously In Ambient Temperature Of 10-55 Deg C And Relative Humidity Of 15-90% Nc ) The Unit Shall Be Capable Of Operating Continuously In Ambient Temperature Of 20- 40 Deg C And Relative Humidity Of 15-90% N 177 23. Documentation Na ) User / Technical / Maintenance Manuals To Be Supplied In English Nb ) List Of Important Spares And Accessories With Their Part Number And Costing N 178 24. Essential Accessories To Be Supplied At Initial Purchase With Each Piece Of Equipment Na ) Reusable Temperature Probes ( Full Set ) : 5 Nos / Per Equipment. 179 25. The Rates Of Consumable Accessories Should Also Be Quoted Separately N26. Onsite Physical Demonstration / Training Of The Equipment To All The End Users With All The Requested Facilities Will Be Mandatory. 180 Icu Beds Nspecification Nsize Approx. 2160Mml X 1020Mmw X 450Mm To 810Mm Height ( Without Mattress ) Nbed Platform Size: 2070Mm L X 960Mm W; Mattress Platform Size: 1900 Mm L X 865 Mm W 181 Five Section Polypropylene Detachable Tops Fitted On Four Section Top Bed Frame With Perforated Design For Easy Breathing Of Mattress 182 Back Rest And Leg Rest Both Shall Have Detachable Mattress Guards ( 3 Nos. On Each Section Respectively ) 183 Back Rest: Min. 45% Of The Frame Length 184 Should Be Able To Adjust Back Rest, Knee Rest, Height Adjustment And Trendelenburg / Reverse Trendelenburg Positions Using Lever. 185 Backrest And Knee Rest Shall Retract As They Are Individually And Simultaneously Raised 186 Bed Frame Shall Be Mainly Made From 50 X 25Mm X 2Mm Thick Erw Tube With Proper Support. 187 This Frame Should Be Fitted On The Base Frame Mainly Made Of 60 X 30 X 1.6Mm Erw Tubes On Various Supporting Links 188 The Base Frame Shall Be Mounted On 125 Mm Dis Non-Rusting Twin Wheel Castor With Central & Directional Locking Mechanism 189 Twin Wheel Castors With Castor Housing And Wheels Made From High Grade Non Floor Staining Synthetic Materials And Integrated Thread Guards. Wheel Centre Having Precision Ball Bearing To Run Smoothly 190 The Bed Shall Have Polymer Moulded Head And Foot Side Panels Detachable By Hand Without Need Of Any Tool. Four Corner Rubber Buffers 191 Bed Shall Have Split Type Swing Down Railing, 2 On Each Side ( Head And Middle Sections ) Made From Polymer Moulded Material. These Shall Be Fitted To The Mattress Support Sections And Should Be Able To Raise And Lock Through Spring Lock Mechanism Through An Operating Lever. When Put Down, They Should Undergo And Level With Bed Frame 192 Railing Shall Avoid Any Finger And Neck Entrapments And Comply With Iec Standards 60601-2-52 193 31.7Mm Dia; 18G Stainless Steel Outer Covering Tube With A Knob To Mount Syringe Pump Nbuilt-In Bed Extension Of Approx. 200Mm Shall Be Provided 194 Accessories: N12mm Diameter Stainless Steel Ss304 Telescopic Heavy Duty Iv Rod With 2 Hooks With Provision To Park When Not In Use Nurine Bag Holder – One Nchart Holder – One N 195 Four Section Mattress With 4 Inch Thick Pu Foam Of 40 Density, Covered With Superior Cover Material ( Water Proof, Anti- Bacterial And Flame Retardant Properties ) Oxygen Cylinder Cage 196 Defibrillator- Cardioverter With Ecg Monitor Nspecification N1 Description Of Function N1.1 Defibrillator Is Required For Reviving The Heart Functions By Providingselected Quantum Of Electrical Shocks With Facility For Monitoringvital Parameters. 197 2 Operational Requirements N2.1 Defibrillator Should Be Bi- Phasic, Light Weight And Latest Model N2.2 Should Monitor Vital Parameters Like Ecg, Heart Rate Etc. And Display Them N2.3 Should Print The Ecg When Required. N2.4 Should Work On Manual Mode ( 0-200J Or More ) . N2.5 Should Be Capable Of Doing Synchronized & Asynchronized Cardioversion Both. N2.6 Can Be Operated From Mains As Well As Battery. N2.7 Should Have Defibrillator Testing Facility. N N 198 2.8 Facility For Trans-Cutaneous Pacing And Trans-Venous Pacing Nshould Be Available N2.9 Demonstration Of The Equipment Is A Must. 199 3 Technical Specifications N3.1 Should Be A Low Energy Biphasic Defibrillator Monitor With Recorder, Having Capability To Arrest All Arrhythmia Within A Maximum Energy Of 200 Joules For Manual Mode. 200 3.2 Should Monitor Ecg Through Paddles, Pads And Monitoringelectrodes And Defibrillate Through Pads And Paddles. Should Have Automatic Or Manual Lead Switching To See Patient Ecg Through Paddles Or Leads 201 3.3 Should Measure And Compensate For Chest Impedance N3.4 Should Have A Built In Printer / Thermal Recorder. N3.5 Should Have Minimal Charging Time For Maximum Energy With Charging Indicator ( Mention The Time In The Bid – Shorter Is Preferred ) . 202 3.6 Should Have Bright Lcd / Tft Display For Viewing Messages And Ecg Waveform N3.7 Adult And Paediatric Paddles Should Be Available N3.8 Should Have Event Summary Facility For Recording, Printing And Patient Data Storage Of Ecg And Events. N 203 3.9 Should Have A Battery Capable Of Usage For At Least 60 Minutes Or 30 Discharges N3.10 Should Be Capable Of Printing Reports On Event Summary, Configuration, Self-Test, Battery Capacity Etc N3.11 Should Have Facility For Self-Test / Check Before Usage And Set Up Function N3.12 3.12 Should Be Capable Of Delivering Energy In Increments Of 1-2 Joules Up To 30J And Increments Of Max. 50J Thereafter. ( Narrow Increments Preferable ) N3.13 Should Have User Friendly Colour Coded Operation. N 204 4 System Configuration Accessories, Spares And Consumables N4.1 Defibrillator -01 N4.2 Paddles Adult & Paediatric -01 Each N4.3 Patient Cable -01 N4.4 Ecg Rolls -5 N4.5 Disposable Pads-5 Nos. N4.6 Complete Set Of Ecg Leads- 02 N4.7 Price Has To Be Quoted Inclusive Of The Above ( 4.1 – 4.6 ) Items And Nseparately For The Accessories And Consumables As Mentioned ( 4.2 – N4.6 ) . N 205 5 Environmental Factors N5.1 The Unit Shall Be Capable Of Being Stored And Operating Ncontinuously In Ambient Temperature Of 10-40?C And Relative Nhumidity Of 15-90%. N 206 6 Power Supply N6.1 Power Input To Be 220-240Vac, 50Hz N6.2 Resettable Overcurrent Breaker Shall Be Fitted For Protection. N 207 7 Standards, Safety And Training N7.1 Should Be Usfda And European Ce Approved Product. N7.2 Electrical Safety Conforms To Acceptable Standards ( Provide Certificate ) N7.3 Should Conform To International Test Protocols On Exposure To Shock Forces And To Vibration Forces. The Standard Should Be Documented. N7.4 Should Have Local Service Facility With Necessary Equipments Recommended By The Manufacturer To Carry Out Preventive Maintenance Test As Per Manual. N 208 8 Documentation N8.1 User Manual & Service Manual In English N8.2 List Of Important Spare Parts And Accessories With Their Part Number And Costing N8.3 Certificate Of Calibration And Inspection From Factory. N8.4 Log Book With Instruction For Daily, Weekly, Monthly Maintenance Checklist. The Job Description Of The Hospital Technician And Company Service Engineer. N 209 8.5 List Of Equipments Available For Providing Calibration And Routine Maintenance Support. N8.6 Compliance Report To Be Submitted In A Tabulated And Point Wise Manner Clearly Mentioning The Page / Para Number Of Original Catalogue / Data Sheet. Any Point, If Not Substantiated With Authenticated Catalogue / Manual, Will Not Be Considered. 210 8.7 Must Submit User List And Performance Report Within Last 5 Years Nfrom Major Hospitals / Government Hospitals. 211 Warranty For 3 Years Namc For 5 Years. 212 Automatic Double Breast Pump Nspecification N1. Unique Programmable Breast Pump Available With Program Card With Initiate, Build & Maintenance Program. 213 2. Breast Pump Should Be Electrical & Battery Operated. N3. Should Have Lcd Display; Equipped Within Internal Rechargeable Batteries. N4. Should Be Made Up Of Hospital Grade Material For Use By Multiple Mothers And Heavy Duty. N 214 5. Parts Should Be Cleanable And Sterilisable Easily Without Any Damage. N6. Double Pump: Must Be Able To Pump Both Breasts At The Same Time To Get More And Better-Quality Milk. N7. Two Phase Expression Technology: Designed To Mimic Baby’S Sucking Pattern To Optimise Milk Output I.E., Stimulation Followed By Expression. 215 8. Should Be A Closed System; Membrane Cap & Diaphragm Should Be Attached To Breast Pump Machine Only. No Diaphragm & Membrane Cap Should Be Attached To Collection Bottle. 216 9. Pump Should Automatically Change Mode After 2 Minutes; Changes From Stimulation To Expression Mode; Along With This, There Should Be Facility To Change Mode Individually. 217 10. Pump Should Be Portable With Weight Of 3-4 Kg N11. Live Demonstration And Training Of End Users For The Equipment Is Must. N12. Catalogue / Brochure Should Be Submitted Along With Technical Bid Mentioning Each And Every Point Of Technical Specification. N13. Pump Should Be European Ce / Us Fda / Iso Approved. N14. Breast Pump Should Have Protection Class Ii, Type B N 218 15. 5 Years’ Comprehensive Warranty. Company Should Ensure The Supply Of Consumables And Accessories For The Period Of Warranty And Cmc. 219 16. Availability Of Spares From Installing Date Must Be There For A Period Of At Least 10 Years. 220 17. The Bidder Must Be A Manufacturer Or Its Authorized Agent. 221 18. Mandatory Accessories / Consumables Should Be From Same Manufacturer: - N• Tubing, Breast Shield- 24Mm, Valve Membrane ) – 40Pcs N• Disposable Milk Collection Bottles 150 Ml : 40 Pcs N• Bottle Stand- 01 N 222 19. Should Construct And Fabricate Four Breast Feeding Chambers In The Designated Breast Feeding Room. 223 20. Documentation N• User / Technical / Maintenance Manuals To Be Supplied In English N• Certificate Of Calibration And Inspection From Factory N 224 21. General Requirement For Electrical Safety Of Medical Equipment. 225 T Piece Resuscitator Nspecification N1. Should Be Manually Operated, Gas Powered Resuscitator With Consistent Peak Inspiratory Pressure ( Pip ) And Positive End Expiratory Pressure ( Peep ) To Infants. 226 2. Should Accept And Deliver Oxygen Concentrations From 21% To 100%. N3. T-Piece Circuit Should Be Connected To Infant Resuscitation Masks Or Endo Tracheal Tubes. N4. The Gas Flow Outlet Should Allow Easy And Secure Connection Of T-Piece Circuit And Humidified T-Piece Circuit. N 227 5. Manometer Range : -10 To 80 Cmh20; ± 2% Accuracy N6. Maximum Pressure Relief : 8L / Min 5 To 70 Cmh20 N7. Peak Inspiratory Pressure : 5L / Min 2 To 70 Cmh20 8L / Min 3 To 72 Cmh20 10L / Min 4 To 73 Cmh20 15L / Min 8 To 75 Cmh20 N8. Input Gas Flow Range : 5L / Min ( Minimum ) To 15L / Min ( Maximum ) N9. Should Be Supplied With The Following Accessory A. Gas Supply Line – 3 Nos N 228 10. Should Be Supplied With The Following Consumables Na. Disposable Infant Resuscitation Tpiece Circuit – 10 Nos Nb. Disposable Infant Resuscitation Tpiece Mask – 10 Nos Nc. Disposable Humidifier T-Piece Circuit With Heated Wire – 10 Nos 229 11. Should Have Safety Certificate From A Competent Authority Ce Issued By Anotified 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 230 Spot Light Nspecification N1. Central Illumination Intensity At A Distance Of 1 Meter: Minimum 30000 Lux N2. Central Illumination Intensity At A Distance Of 0.5 Meter: Minimum 70000 Lux 231 3. Light Field Diameter At A Distance Of 1 Meter: Minimum 165Mm N4. Light Field Diameter At A Distance Of 0.5 Meter: Minimum 110Mm N5. Color Temperature: Minimum 4500 K N6. Color Rendering Index ( Ra ) In Every Color Temperature Setting: 90 Or More N7. Led Life Time: Minimum 50000 Hours N 232 8. Should Be Mounted On Stable Mobile Stand With At Least Five Wheels. N9. Stand Should Have Hinged Arm On Which The Light Is Mounted. N10. Light Should Be Height Adjustable And Angle Adjustable. N11. Class Ii Medical Electrical Equipment Protection ( Iec 60601-1 ) N 233 12. Light Housing Ingress Protection Class ( Iec 60601-1 & Iec 60601-2-2 ) : Ip20 Or Better N13. System Should Have Bis / Us Fda / European Ce With Four-Digit No. Certificate For The Intended Use. 234 Cardiac Table
