User`s Manual - Frank`s Hospital Workshop
Contents
1. AA Alkaline Batteries To power VENTY from AA alkaline batteries insert seven disposable alkaline batteries Panasonic AM3X or equivalent into the Battery Case Cat No 6862 00 following the polarity markings on the case WARNING Do not recharge or incinerate alkaline batteries Attempting to do so may cause the batteries to leak or explode Rechargeable Battery VENTv can operate from the optional Duracell DR30 or equivalent rechargeable battery If a rechargeable battery has not been used for three months or more recharge it before use WARNING Battery can explode leak or catch on fire if heated or exposed to fire or high temperatures Additional Battery Information e Dispose of batteries in accordance with local laws e Do not mix battery types e g disposable and rechargeable AA batteries e VENTV may not power up if the batteries are nearly depleted To install or remove the battery grasp the finger grips on each end of the VENTV battery cover Squeeze together and pull so that the hinged cover opens The battery is keyed and can be installed in only one orientation see illustration inside 10 VENTV User s Manual Rev 02 battery compartment The contacts should go in first and be located toward the top left of the monitor Close the battery cover before operating the monitor Connect only Novametrix approved devices Swing battery cover open Hinged Battery Com2. sensor that converts volumetric flow rate into a differential pressure signal Gas flowing through the flow sensor causes a small pressure drop across the two ports connected to the sensor This pressure drop is transmitted through the tubing to the monitor where differential and absolute pressure transducers are located This pressure drop is correlated to flow according to the factory stored calibration The relationship between the volumetric flow rate and the resulting differential pressure is governed by standard fluid mechanics equations User calibration is not required because of the ability of the plastic injection mold to produce precision flow sensors Empirical calibration for the specific pneumotach type pediatric adult neonatal etc is performed at the factory and is stored in the monitor The pressure transducer is automatically zeroed to correct for changes in ambient temperature electronics and position gravity effects VENTV User s Manual 5 Keep the VENTV and its accessories clean Do not operate the VENTW when it is wet due to spills or condensation Patient Safety Connect only Novametrix Series 3 Flow Sensors to the VENTV For maximum performance keep the pressure sensor ports oriented upward and keep the sensor clear of moisture and secretions by proper breathing circuit maintenance Connect the sensor first to the VENTV and then to the patient breathing circuit in order to limit circuit volume loss and to
3. 02 Key Action Function 1 on Press Turns VENTY on off Ae Display Graph Screens 2 Press Additional presses causes VENTY to sequence through available Graph Screens Display Data Screens 3 DATA Press Additional presses causes VENTY to sequence through available Data Screens Press Turns display backlight on off oy 4 P Press amp Adjusts contrast viewing angle of display Hold 1 step sec Illuminated if powered from battery A L None Green battery charged 9 Yellow flashing slowly capacity getting low Red flashing quickly exhausted in 10 15 min B NEO None Illuminates when a Neonatal sensor is O connected Symbol Description Patient Isolation Identifies patient isolation connection as type BF AN Attention Consult manual for detailed information VENTW User s Manual 9 Power supply options Battery Installation The VENTY can be powered from seven AA disposable alkaline batteries or a rechargeable battery Battery capacity is shown in the chart below it may be reduced in colder temperatures or with power cycling and slightly increased if VENTV is operated with its backlight off Standard Optional AA alkaline batteries Rechargeable battery 7 ea disposable NiMH 7 2 vdc is PA Power Source Capacity continuous 8 hours 12 hours Recharge Time n a 1 5 hours 400038 battery 6862 00 case Catalog Number 400043
4. avoid excessive moisture build up in the flow sensor tubing VENTV has electrically isolated inputs Patient leakage current flowing from the instrument to ground is limited to less than 50 uA at 120 V 60 Hz Patient isolation is greater than 10 MQ 2500 V rms at 60 Hz Where electromagnetic devices i e electrocautery are used patient monitoring may be interrupted due to electromagnetic interference Electromagnetic fields up to 3 V m will not adversely affect system performance VENTY contains no user serviceable parts Refer servicing to qualified service personnel See Accessories on page 21 for listings of the Service Manual and Service Test kit for use by technical personnel e This product and its accessories which have patient contact are latex free Warnings WARNING Indicates a potentially harmful condition that can lead to personal injury e Explosion Hazard Do NOT use the VENTV in the presence of flammable anesthetics Use of this instrument in such an environment may present an explosion hazard e Electrical Shock Hazard Always turn the monitor off before cleaning it Do NOT use a damaged monitor or sensor Refer servicing to qualified service personnel e Fire Hazard The VENTY should not be exposed to elevated oxygen levels at elevated pressures Use in such an environment may present a fire hazard e Failure of Operation If the monitor fails to respond as described do not use it until
5. 5 grams 21 0z with rechargeable battery 710 grams 25 oz e Operating Environment 10 to 40 C 50 104 F 10 to 90 relative humidity non condensing e Transport Storage Environment 10 to 55 C 14 131 F 10 to 95 relative humidity non condensing Display Liquid Crystal Display e 128 x 64 pixels 2 5x 1 25 inches e Adjustable contrast with backlight and plastic shield Rev 02 VENTV User s Manual 19 Indicators Alerts AA Alkaline batteries Rechargeable Battery External Battery Charger LED indicators e Remaining battery capacity green yellow red e Neonatal flow sensor connected green Alerts for measured patient parameters None Very low battery alert audible and visual Panasonic AM3X or equivalent 7 required e Type AA Alkaline 1 5 vdc 1500 mAH e Continuous battery life 8 hours minimum at 21 C 70 F e Up to 85 capacity remaining after 4 years storage at 21 C 70 F e Recharge Disposable do not recharge Duracell DR30 or equivalent e Type DR30 Nickel Metal Hydride NiMH 7 2 vdc 2400 mAH gt 250 cycles e Continuous battery life 12 hours minimum at 21 C 70 F e Up to 70 capacity remaining after 30 days storage at 21 C 70 F e Charge Conditions O to 45 C 32 to 113 F e Discharge Conditions 20 to 50 C 4 to 122 F e Recharge time 1 5 hr with external charger Charger compatible with Duracell DR30 or equivalent battery e S
6. IP 20 Platf e Breath by breath reporting MAR PREF e If auto PEEP is detected the word 9 5 auto appears under PEEP and the display reflects total PEEP present A E e Activity bar is breath by breath using Pressure Graph scale TIMING DATA Ti 1 g Te 3 q e Breath by breath reporting e Activity bar is breath by breath using Flow Graph scale DATA GD DATA N GD DATA LI 12 oo GD FLOW VOLUME DATA PIF 36 UTi 533 e Breath by breath reporting FEF 57 UTe 506 ELO AJOLUME DATA A GD MECHANICS DATA Rau 16 RSBI p e Breath by breath reporting conga HIP 0 e RSBI Pediatric Adult sensor in use blank when Neonatal sensor in use DATA al GD e Activity bar is breath by breath using Flow Graph scale Rev 02 VENTV User s Manual 15 GRAPH Each of the graph screens is shown below Display Screens VOLUME GRAPH a e Automatically scaled e Breath by breath reporting PRESSURE GRAPH e Automatically scaled e Breath by breath reporting FLOW GRAPH e Automatically scaled e Breath by breath reporting FLOW VOLUME GRAPH e Automatically F scaled e 4 breaths overlayed then cleared V e Breath by breath PRESSURE VOLUME GRAPH e Automatically y 5 Raw 16 0 scaled Odun I4 0 e 4 breaths overlayed RSET 4 then cleared P o e Breath by breath e RSBI Pediatric Adult sensor in use blank when Neonatal sensor in use System E
7. WIST VT e NOVAMETRIX 4 Vi SU JA lj MECHANICS HANDHELD RESPIRATORY MECHANICS MONITOR VentCheck Model 101 October 30 1997 Catalog No 6800 23 02 Copyright 1997 Novametrix Medical Systems Inc 5 Technology Drive Wallingford Connecticut U S A 06492 All rights reserved About this manual This manual is written for clinical personnel using the VENTY VentCheck Handheld Respiratory Mechanics Monitor Model 101 and the flow sensors and accessories intended for use with the monitor This document contains information which is proprietary and the property of Novametrix Medical Systems Inc and may not be reproduced stored in a retrieval system translated transcribed or transmitted in any form or by any means without the prior explicit written permission of Novametrix Medical Systems Inc Novametrix reserves the right to change specifications without notice VentCheck and the VENTY logo are trademarks of Novametrix Medical Systems Inc VENTv Technical Description Per requirements of IEC 601 1 VENTV is classified as class II equipment internally powered with type BF applied part and an enclosure protection rating of IPX1 Transport Storage 10 to 55 C 14 131 F 10 95 R H non condensing Operating Conditions 10 to 40 C 50 104 F 10 90 R H non condensing The VENTV VentCheck Handheld Respiratory Mechanics Monitor Model 101 contains no user serviceable parts Refer servicing to qua
8. automatic zero self calibration periodically and as needed During this time monitoring is interrupted for less than three seconds The instructions below assume the VENTY has a charged battery installed and that no flow sensor is connected Use of equipment other than mentioned here may yield different results 1 Press the POWER key to turn VENTY on or off Ho SEHSOR DETECTED 2 Verify both the NEO and battery INSERT FLOW SENSOR indicators illuminate as part of the a O self test performed at power up MS Cat Ho 3 Press and hold the LAMP key to naa coe adjust the contrast viewing angle of the display 4 If desired press the LAMP key to turn the display backlight on off 5 Verify INSERT FLOW SENSOR message appears 6 Select a Series 3 Flow Sensor based on the patient type 6717 Pediatric Adult sensor adds approximately 6 5 cc of deadspace 6718 6720 Neonatal sensors add approximately 0 8 cc of deadspace ET Tube Size Series 3 Flow Sensor gt 6 mm e Pediatric Adult Neonatal Pediatric Adult e Pediatric Adult if weight 210 Sensor Sensor 4 5 to 5 5 kg and Vy gt 100 ml 6718 6720 6717 mm e Neonatal if weight lt 10 kg or Vr lt 100 ml lt 4 mm Neonatal 12 VENTV User s Manual Rev 02 Patient Connection Rev 02 7 Remove the sensor from the package Verify the sensor is clean dry and physically intact with no broken edges or disconnected tubing Connect the Flow sens
9. care The device is intended for short term use nominally 1 hour and is NOT intended for continuous monitoring VENTV compatible flow sensors are a single patient use devices having fittings that comply with ISO 5356 1 and may be used in conjunction with endotracheal tubes face masks and breathing circuit devices that also comply with the specification Pediatric adult flow sensors are indicated for use with endotracheal tubes with internal diameters of gt 6 mm Neonatal flow sensors are indicated for use with endotracheal tubes with internal diameters of lt 4 mm Further for endotracheal tubes with internal diameters of 4 5 to 5 5 mm in general neonatal sensors are indicated if the patient weight lt 10 kg or tidal volume lt 100 ml and pediatric adult sensors are indicated where patient weight gt 10 kg and tidal volume gt 100 ml VENTV is intended for short term use nominally 1 hour and is NOT intended as a continuous monitoring device VENTYV does NOT compensate for the presence of high oxygen concentrations anesthetic gases or helium oxygen mixtures When such mixtures are present errors in flow measurements may exist VENTV measures the respiratory parameters of flow and pressure Many other parameters are calculated from the flow and pressure signals including volume tidal and minute airway resistance and lung compliance VENTW uses fixed orifice differential pressure pneumotachs The pneumotach is the airway flow
10. ion periodically and as needed During this time monitoring is interrupted for less than three seconds The automatic zero can be manually initiated by simultaneously pressing the DATA and GRAPH keys After changing the sensor from Adult to Neonatal while the VENTv is operational wait 30 seconds then perform an automatic zero This product and its accessories which have patient contact are free of latex The Cz9 C Compliance Ratio neonatal parameter is not supported To determine the VENTY software version turn the monitor on During the self test performed at power up the software level is shown on the third line as main 101 xx where xx is the software version Some VENTY monitors were produced with the statement Use only Novametrix approved devices 13 VDC 1A located on the label at the Flow Sensor Input Connector This erroneous statement does NOT apply to the VENTY monitor and should be ignored VENTW User s Manual 7 Preparation for Use Getting The VENTY Handheld Respiratory Mechanics Monitor Model 101 is shown below Acquainted Front View Display K amp Connect Series 3 Flow Sensor Flow Sensors VENT NOVAMETRIX Were Neonatal Pediatric Adult Sensor Sensor 6718 6720 6717 Side Bottom View PRN Features Connector Battery Access Quick Guide Compartment Rev 02 8 VENTv User s Manual Keypad Controls and Indicators Symbols Rev
11. li a 11 Monitor Operation stos wt TA AAA AA 12 Power OMO o oooooo ee ee 12 FIOW SONS emita Baw EE Es She A SA erat Bnet 12 Patient Connecti cari a wa de ag a a a 13 Patient DISCONNECE cia di el he Fede wt Bae ees gee hse 14 Screen Display Flowchart 0 ooo ooo 14 DATA Display Screens 1 a 15 GRAPH Display ScreenS 1 a 16 System Errors somaa Rog hot tars A AA whieh ole does ave ee ode 16 Parameter Alerts iii a o Be a E eee 17 Battery Alert aia bof bed wae Ra eR eed wi ee A A 17 Cleaning and Disinfecting 00 cc ee 17 Parameter Listi ar a o Pe a Rae a nee a Pent enon 18 Specifications stich esa a eee wo we eee eae Ra bees 19 ACCESSOS i a Anise A GR es eee Eee Make SG ae es 21 Ml RR 22 VENTV User s Manual 3 4 VENTV User s Manual Rev 02 Indications for Use Contra indications Principles of Operation Rev 02 General Description The VENTV VentCheck Handheld Respiratory Mechanics Monitor Model 101 from Novametrix Medical Systems Inc is an easy to operate stand alone respiratory mechanics monitor It is intended to be used in patient monitoring environments by technically skilled clinical personnel VENTV is indicated for use by technically skilled clinical personnel as a mechanics monitor for mechanically ventilated or spontaneously breathing persons in monitoring environments including the intensive care unit ICU the operating room OR and in emergency transport
12. lified service personnel See Accessories on page 21 for listings of the Service Manual and Service Test kit for use by technical personnel Declaration of Conformity with European Union Directive The Authorized Representative for Novametrix equipment is D R M Green European Compliance Services Limited Oakdene House Oak Road Watchfiled Swindon Wilts SN6 8TD United Kingdom Manual Revision History 31 Jul 97 Release at Rev 00 17 Oct 97 Rev 01 Including software release version 1 1 30 Oct 97 Rev 02 Including software release 1 2 2 VENTV User s Manual Rev 02 Rev 02 Table of Contents General Description ce es 5 Indications for Use oi rewi ooo ooo ooo 5 Contra indi ations siii Ga a a a a a 5 Principles of Operation lt o omiani ooo e an a o aa a E E a a O aa 5 Patient Safety ora A a AE A ae E AE eee 6 Warnings ienien maoa aaa ES A AA aw An aE Fe 6 CAUTIONS ouar Ok eS A A E ee T ak eS ee eee aa a 7 NOTES 5 da ah a alee ate x rt Raed tte te ie Aine ee ops BE de aetna ate 7 Pr paration for Use Li eG Ae ed and dae ek dale en Awa ee 8 Getting Acquainted 3402 ra beet eae eee bh Pad Ge bare et 8 Keypad Controls and Indicators 0 0c a es 9 SYMBDO S ssa ees Ao id eek eek end Betta A ae ee PE ee ek a oa eS 9 Power supply options 1 ce nnana aana 9 Battery Installation 1 es 10 External Battery Charger 000 ee 11 Features Connector oa ce aaae a ee Pee
13. o VENTW a E Point tubing Pediatric Adult To ventilator Flow Sensor Neonatal Flow Sensor To patient To patient VENTW User s Manual 13 Patient Disconnect Screen Display Flowchart VENTV does NOT provide audible alarms and will not alert the user to inadvertent disconnection of the flow sensor from either the breathing circuit of the monitor s sensor input connector NOTE To limit circuit volume loss and avoid excessive moisture build up in the flow sensor tubing disconnect the flow sensor from the breathing circuit before disconnecting the flow sensor from the monitor 10 Press the GRAPH or DATA keys and the most recently viewed data or graph screen appears in the display Additional key presses cause VENTY to sequence through the available data screens as shown below a a E Mech 586 12 6 1 12 6 1 S E E 4 0 f s Wile RES MU 6 8 S E b 3 B i PIP 28 PEEP 5 A a hie has 0 gr 12 O E FEF 57 UT e 506 FLOW WOL UME S E S E F aa 16 RSBI p dinga HIP 0 a ERE 1 Raw 16 0 Coen 34 8 RSHI al on 14 VENTV User s Manual Rev 02 DATA Each of the data screens is shown below pata Display Screens VOLUME DATA e Spon spontaneous breath Mech mechanical breath e Values from rolling 8 breath aver age e Activity bar is breath by breath using Volume Graph scale PRESSURE DATA P
14. or to the VENTV e Verify VENTY briefly displays the selected sensor type e Verify the NEO indicator is illuminated only if a neonatal sensor is in use After connecting the flow sensor to the VENTY place the flow sensor into the breathing circuit proximal to the patient NOTE Connect the sensor first to the monitor and then to the patient breathing circuit in order to limit circuit volume loss and to avoid excessive moisture build up in the flow sensor tubing The sensor is best placed between the endotracheal tube and the ventilator circuit wye Do NOT position the sensor between the ET tube and the elbow pediatric adult circuit as this may allow patient secretions to build up in the sensor If other airway appliances e g suction adapter elbow heat moisture exchanger HME CO adapter etc are in use place the flow sensor in the more distal position away from the patient closer to the circuit wye To prevent rain out and moisture from draining into the sensor do NOT place the sensor in a gravity dependent position where moisture and secretions may accumulate Periodically check the flow sensor and tubing for excessive moisture and or secretion build up After changing the sensor from Adult to Neonatal while the VENTY is operational wait 30 seconds then perform an automatic zero by simultaneously pressing the DATA and GRAPH keys To VENTV To ventilator Point tubing T
15. partment Cover Finger Grips External Battery An optional external charger for the Duracell DR30 is available The external charger allows the battery to be recharged outside of the VENT monitor e The external charger is for use with the rechargeable Duracell DR 30 battery only e Ina non patient area connect the external charger to an AC source Remove the battery from the VENTY and insert it into the external charger The battery will be fully charged in approximately 1 1 2 hours e Refer to the instructions supplied with the charger for additional information WARNING The external battery charger should NOT be operated near or in close proximity to patients and or other medical equipment in operation Charger The VENTV features connector is for use only with future optional Novametrix accessories The connector meets the patient safety requirements set forth by the safety agencies as labelled on the VENTW monitor Features Connector Rev 02 VENTV User s Manual 11 Power On Off Flow Sensor Monitor Operation Prior to operating the VENTY monitor please note the following e VENTY is intended for short term use nominally 1 hour and is NOT intended as a continuous monitoring device e VENTV does NOT compensate for the presence of high oxygen concentrations anesthetic gases or helium oxygen mixtures When such mixtures are present errors in flow measurements may exist e The VENTV performs an
16. r illuminates GREEN to indicate a charged battery slowly flashes YELLOW to indicate capacity is getting low and quickly flashes RED to indicate the battery will become exhausted within 10 15 minutes When the battery indicator flashes RED VERY LOW BATTERY appears in the title stripe area of the display example at right WERY Lok BATTERY e Turn VENTY off before cleaning Do not immerse the monitor Do not attempt to sterilize the monitor e The monitor can be cleaned and disinfected with solutions such as isopropyl alcohol 70 solution 2 glutaraldehyde solution or bleach 10 solution then wiped with a clean water dampened cloth to rinse and dry before use e Treat Series 3 Flow Sensor in accordance with established protocol for single patient use items VENTV User s Manual 17 Parameter List Parameters reported by the VENTY are summarized below 18 VENTv User s Manual Abv Units Parameter Cdyn ml cmH20 Dynamic Compliance I E Inspiratory Expiratory Ratio MAP cmH 20 Mean Airway Pressure MV Liters Minute Volume NIP cmH 0 Negative Inspiratory Pressure PEEP cmH 0 Positive End Expiratory Pressure PEF LPM L min Peak Expiratory Flow PIF LPM L min Peak Inspiratory Flow PIP cmH 20 Peak Inspiratory Pressure Plat cmH 0 Plateau Pressure Raw cmH gt O L sec Airway Resistance RR br min Respiratory Rate RSBI br min L Rapid Shallow Breathing Index Te sec Expi
17. ratory Time Ti sec Inspiratory Time VT ml Tidal Volume Averaged VTi ml Tidal Volume Inspiratory VTe ml Tidal Volume Expiratory Rev 02 Specifications Below are specifications for the Novametrix VENTY Handheld Respiratory Mechanics Monitor Model 101 These specifications are listed for informational purposes only and are subject to change without notice Principle of Fixed orifice differential pressure pneumotach No calibration required Operation Flow Sensors Series 3 Flow Sensors Single Patient Use ET Tube Size Series 3 Flow Sensor Catalog No gt 6 mm Pediatric Adult 6717 4 5 5 5 mm Pediatric Adult if weight 210 kg and Vy 2100 ml 6717 i Neonatal if weight lt 10 kg or V lt 100 ml 6718 6720 lt 4 mm Neonatal 6718 6720 Flow e Range Adult Sensor 2 to 180 L min Range Neonatal Sensor 0 25 to 35 L min Accuracy Greater of 0 5 L min or 5 of reading pediatric adult sensor Greater of 0 125 L min or 5 of reading neonatal sensor Pressure e Range 120 to 120 cmH 0 Accuracy Greater of 0 5 cmH gt 0 or 2 of reading Respiratory Rate e Range O to 120 br min Accuracy 1 br min Resolution 1 br min Sensor Type Identification Automatic Automatic Barometric Pressure Compensation 400 800 mmHg Physical VENTY monitor e Size maximum height width depth 20 x9 5 x4 8 cm 8x3 75x1 875 in e Weight typical without battery 370 grams 13 oz with alkaline battery pack 59
18. rrors If VENTY detects that a system error has occurred patient monitoring is interrupted and an error message is displayed Correcting the error SYSTEM ERROR A condition will clear the error message from the display and monitoring will resume The CALL SERVICE messages cannot be cleared from the display without power cycling the monitor INVALID SENSOR TYPE 16 VENTV User s Manual Rev 02 Parameter Alerts Battery Alert Cleaning and Disinfecting Rev 02 The following errors are possible Possible Error Message Corrective Action g Cause CALL SERVICE Faulty monitor Remove monitor and flow sensor or sensor from use Contact qualified service personnel and note number shown in triangle INVALID SENSOR TYPE Incorrect sensor type connected Replace sensor with a valid sensor type pediatric adult or neonatal Damaged Connector is damaged Replace sensor sensor Damaged Monitor s sensor connector is monitor damaged Remove from use and contact qualified service personnel FLOW OUT OF RANGE Flow rate VENTV does not operate with flow greaterthan 180 rates in excess of 180 L min L min PRESSURE gt 120 CM H20 Pressures gt 120 cm H20 were detected Do not expose monitor sensor to pressures in excess of 120 cm H20 VENTY does not provide audible or visible parameter alerts VENTY monitors and indicates to the user the remaining battery capacity The battery indicato
19. the situation has been corrected by qualified personnel e Do not apply tension to the sensor tubing while connected to a patient breathing circuit as accidental extubation may result e Do not position the flow sensor s tubing in any manner that may cause entanglement or strangulation e Use the optional external battery charger in non patient areas only 6 VENTY User s Manual Rev 02 Cautions Notes Rev 02 CAUTION Indicates a condition that may lead to equipment damage or malfunction e Federal U S A law restricts this device to sale distribution or use by or on the order of a licensed medical practitioner e Electrical Shock Hazard Always turn the monitor off before cleaning Do NOT use a damaged monitor e Do NOT use a damaged flow sensor e Do NOT immerse the monitor or sensors in liquids e Do NOT sterilize the monitor or the sensors e No user serviceable parts inside Refer servicing to qualified service personnel e Operate at temperatures between 10 C to 40 C 50 104 F lt 90 relative humidity non condensing e Avoid storing the monitor at temperatures less than 20 C or greater than 55 C lt 4 F or gt 131 F NOTE Indicates points of particular interest or emphasis and intended to provide for more efficient or convenient operation e The VENTVY operates with Novametrix Series 3 Flow Sensors only e The VENTY performs an automatic zero self calibrat
20. torage Conditions 40 to 70 C 40 to 158 F e Operating Conditions O to 50 C 32 to 122 F optimum 25 C 77 F e Recharge time 1 5 hour typical 20 VENTY User s Manual Rev 02 Accessories Cat No Description Monitor English language 6800 00 VENTV Handheld Respiratory Mechanics Monitor Model 101 6800 23 User s Manual 6800 90 Service Manual VENTY Quick Guide Inservice Video 420037 VHS video tape NTSC format U S A 420038 VHS video tape PAL format 420039 VHS video tape SECAM format Flow Sensors 6717 00 Series 3 Pediatric Adult Flow Sensor 10 Box 6718 00 Series 3 Neonatal Flow Sensor 10 Box 6720 00 Series 3 Neonatal Combined CO gt Flow Sensor 10 Box Power Options 6862 00 Battery Case for AA Batteries batteries not included 400038 Alkaline Battery 1 5 vdc AA Size Panasonic AM3X or equivalent 400043 Rechargeable Battery NiMH 7 2V 2 4AH Duracell DR30 or equivalent 400049 External Battery Charger DR30 Universal Voltage NiMH power line cord not included 600026 Power Line Cord 120 vac U S A for External Battery Charger Miscellaneous 140084 Pole Shelf Mount Kit 315107 Carrying Case Rev 02 VENTV User s Manual 21 Warranty Equipment manufactured or distributed by Novametrix Medical Systems Inc is fully guaranteed covering materials and workmanship for a period of one year from the date of shipment except for certain disposable products and products
21. with stated guarantees other than one year Novametrix reserves the right to perform guarantee service s at its factory at an authorized repair station or at the customer s installation Novametrix obligations under this guarantee are limited to repairs or at Novametrix option replacement of any defective parts of our equipment except fuses batteries and calibration gasses without charge if said defects occur during normal service Claims for damages during shipment must be filed promptly with the transportation company All correspondence concerning the equipment must specify both the model name and number and the serial number as it appears on the equipment Improper use mishandling tampering with or operation of the equipment without following specific operating instructions will void this guarantee and release Novametrix from any further guarantee obligations Service Department For factory repair service Call toll free 1 800 243 3444 To Call Direct 203 265 7701 Facsimile 203 284 0753 http www novametrix com techline novametrix com Caution Federal U S A law restricts this device to sale distribution or use by or on the order of a licensed medical practitioner Copyright 1997 Novametrix Medical Systems Inc 5 Technology Drive Wallingford Connecticut 06492 All rights reserved 22 VENTY User s Manual Rev 02
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