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1. visiefiAire WARNING SMOKING WHILE USING OXYGEN IS THE NUMBER ONE CAUSE OF FIRE INJURIES AND RELATED DEATHS YOU MUST FOLLOW THESE SAFETY WARNINGS WARNING DO NOT ALLOW SMOKING CANDLES OR OPEN FLAMES IN THE SAME ROOM WITH THE DEVICE OR THE OXYGEN CARRYING ACCESSORIES WARNING SMOKING WHILE WEARING AN OXYGEN CAN NULA MAY CAUSE FACIAL BURNS AND POSSIBLY DEATH WARNING IF YOU SMOKE THESE 3 STEPS MAY SAVE YOUR LIFE TURN OFF THE OXYGEN CONCENTRATOR TAKE OFF THE CANNULA AND LEAVE THE ROOM WHERE THIS DEVICE IS LOCATED WARNING NO SMOKING OXYGEN IN USE SIGNS MUST BE PROMINENTLY DISPLAYED IN THE HOME OR WHERE OX YGEN IS IN USE PATIENTS AND THEIR CAREGIVERS MUST BE INFORMED ABOUT THE DANGERS OF SMOKING IN THE PRESENCE OF OR WHILE USING MEDICAL OXYGEN WARNING DO NOT USE YOUR OXYGEN CONCENTRATOR IN THE PRESENCE OF FLAMMABLE GASES THIS CAN RESULT IN RAPID BURNING CAUSING PROPERTY DAMAGE BODILY INJURIES OR DEATH WARNING REMOVING THE CANNULA AND PUTTING IT ON CLOTHING BEDDING SOFAS OR OTHER CUSHION MATERIAL WILL CAUSE A FLASH FIRE WHEN EXPOSED TO A CIGARETTE HEAT SOURCE OR FLAME WARNING DO NOT LEAVE A NASAL CANNULA ON OR UNDER CLOTHING BED COVERINGS OR CHAIR CUSHIONS IF THE UNIT IS TURNED ON BUT NOT IN USE THE OXYGEN WILL MAKE THE MATERIAL FLAMMABLE SET THE OXYGEN CONCENTRATOR TO THE 0 OFF POSITION WHEN THE OXYGEN CONCENTRATOR IS NOT IN USE CAUTION Always place oxygen supply tubing and power c
2. Immunity test IEC 60601 test level Electromagnetic environment guidance level Electromagnetic environment guidance IEC 61000 4 2 Electrical fast transient burst IEC 61000 4 4 Surge IEC 61000 4 5 Voltage dips short interruptions and voltage variations on power supply input lines IEC 61000 4 11 Power frequen 50 60 Hz magnetic field IEC 61000 4 8 6 kV contact 8 kV air 2 kV for power supply lines 1 kV for input output lines 1 kV line s to line s 2 kV line s to earth 5 U gt 95 dip in U for 0 5 cycle 40 U 60 dip 0 for 5 cycles 70 U 30 dip in U for 25 cycles 5 U gt 95 dip U for 5 sec 6 kV contact 8 kV air 2 kV for power supply lines N A 1 kV line s to line s 5 U gt 95 dip U for 0 5 cycle 40 U 60 dip in U for 5 cycles 70 U 30 dip in U for 25 cycles 5 U gt 95 dip in U for 5 sec Floors should be wood concrete or ceram ic tile If floors are covered with synthetic material the relative humidity should be at least 30 Mains power quality should be that of a typical commercial or hospital environment Mains power quality should be that of a typical commercial or hospital environment Mains power quality should be that of a typical commercial or hospital environment If the user of the unit requires continued operation du
3. Concentration Indicator optional mandated for EU and specific countries When equipped with an Oxygen Monitor a warning LED amber is activated on the front panel see Safety Features for details Hour Meter Records the concentrator s cumulative hours of operation Operating Instructions Label Directs usage of the unit Casters Four casters enable unit to be easily moved as needed Specification Label Displays electrical specifications and serial number VisionAire 2 amp 3 User Manual 9 visiefiAire Humidifier Bottle optional Humidifier Bottle Recess Humidifier Bottle Fitting Humidifier Bottle Tubing Humidifier Bottle Oxygen Outlet Humidifier Bottle Oxygen Tubing Cannula a Power Cord Power Cord Allows connection of the unit to an Humidifier Bottle optional Humidifies the oxygen electrical outlet before it reaches the patient Humidifier Bottle Recess Area to place the optional Humidifier Bottle Oxygen Outlet Connection for humidifier bottle oxygen tubing cannula 10 MN165 1 H VisiohAire Accessories Safety Features Recommended for use with VisionAire 2 and Miri Pat Safety Feature VisionAire 3 Compressor Thermal safety is ensured by a The use of certain administration accessories which Motor thermostat situated in the stator are not specified for use with this concentrator may winding 135 C 275 A reduce performance and void the manuf
4. and understand the concentrator labeling and instructions for use then use is recommended only under the supervision of one who can If any discomfort is felt while using the concentrator patients are advised to contact their healthcare provider Patients are also advised to have back up oxygen available i e cylinder oxygen in the event of a power outage or concentrator failure There are no other unique skills or user abilities required for concentrator use Concentrator Components Review the figures below and become familiar with the important parts of your VisionAire 2 or VisionAire 3 Oxygen Concentrator Front of Concentrator Oxygen Outlet Flowmeter Adjustment Knob Low Oxygen Concentration Indicator optional mandated for EU and specific countries VisionAire 2 Caster s Top and Side Handles Enables convenience in carrying the unit On Off 1 0 Power Switch Starts and stops the operation of the unit Oxygen Outlet Provides connection for a humidifier if required or cannula Circuit Breaker Reset Button Resets the unit after electrical overload shutdown Flowmeter Adjustment Knob Controls the oxygen flow rate in liters per minute LPM oo UP R 4 VisiefiAire Top Handle Hour Meter Side Handle s Circuit Breaker Reset Button ON OFF 1 0 Power Switch Operating Instructions Label EP d Specification Label Low Oxygen
5. are at least 1 foot 30 cm away from a wall or other obstruction Do not place the unit in a confined area Choose a dust and smoke free location away from direct sunlight Do not operate the unit outdoors unless the unit is plugged into a Ground Fault Interrupter GFI protected outlet Locate the unit near the electrical outlet in the room where you spend most of your time 2 Insert the power cord plug into the electrical outlet 3 Set the 1 0 power switch to the T position to turn the unit on An audible alarm will loudly sound for approximately 5 seconds 4 The low oxygen concentration indicator remains on for a few minutes and until the oxygen concentration reaches minimum concentration requirements only pertains to unit equipped with an Oxygen Monitor Un To set the flow of supplemental oxygen turn the flowmeter adjustment knob left or right until the ball inside the flowmeter centers on the flow line number prescribed by your physician To view the flowmeter at the proper angle note that the back line and the front number line must give appearance of one line 6 The concentrator is now ready for use Note Optimal oxygen concentration is obtained within 10 minutes after the device is switched on 9096 of the concen tration is obtained after approximately 5 minutes CAUTION It is very important to select only the prescribed level of oxygen Do not change the e flow selection unless yo
6. or cold water distilled water is preferred to the fill line indicated on the bottle DO NOT OVERFILL 4 Re connect the top cover to the humidifier bottle 5 Place the humidifier bottle in the humidifier bottle recess on the back of the concentrator and connect the humidifier bottle tubing to the oxygen outlet and the humidifier bottle fitting CAUTION If the humidifier bottle tubing is not properly connected to the humidifier bottle fitting or to the oxygen outlet an oxygen leak can occur Cannula Connection Connect the tubing and cannula to the unit s oxygen outlet or to the optional humidifier s oxygen outlet 12 MN165 1 H Starting the Concentrator WARNING NO SMOKING OXYGEN IN USE SIGNS MUST BE PROMINENTLY DISPLAYED IN THE HOME OR WHERE OXYGEN IS IN USE PATIENTS AND THEIR CAREGIVERS MUST BE INFORMED ABOUT THE DANGERS OF SMOKING IN THE PRESENCE OF OR WHILE USING MEDICAL OXYGEN WARNING DO NOT USE EXTENSION CORDS WITH THIS UNIT OR CONNECT TOO MANY PLUGS INTO THE SAME ELECTRICAL OUTLET THE USE OF EXTENSION CORDS COULD ADVERSELY AFFECT THE PERFORMANCE OF THE DEVICE TOO MANY PLUGS INTO ONE OUTLET CAN RESULT IN AN OVERLOAD TO THE ELECTRICAL PANEL CAUSING THE BREAKER FUSE TO ACTIVATE OR FIRE IF THE BREAKER OR FUSE FAILS TO OPERATE CAUTION Position the unit away from curtains or drapes hot air registers or heaters Be certain to place the unit on a flat surface and make sure all sides
7. than the compliance level in each frequency range Interference may occur in the vicinity of equipment marked with the following symbol NOTE 1 At 80 MHz and 800 MHz the higher frequency range applies NOTE 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people a Field strengths from fixed transmitters such as base stations for radio cellular cordless telephones and land mobile radios amateur radio AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy To assess the electromagnetic environment due to fixed RF transmitters an electromagnetic site survey should be considered If the measured field strength in the location in which the VisionAire is used exceeds the applicable RF compliance level above the VisionAire should be observed to verify normal operation If abnormal performance is observed additional measures may be necessary such as re orienting or relocating the VisionAire Over the frequency range 150 kHz to 80 MHz field strengths should be less than 3 V m VisionAire 2 amp 3 User Manual 17 visiefiAire Recommended separation distances between portable and mobile RF communications equipment and the unit The unit is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled The customer or the user of the unit can help p
8. unit so that it is difficult to access the power cord CAUTION The concentrator should be located as to avoid smoke pollutants or fumes CAUTION Ensure concentrator is operated in an upright position CAUTION Always place oxygen supply tubing and power cords in a manner that prevents a trip hazard CAUTION Position the unit away from curtains or drapes hot air registers or heaters Be certain to place the unit on a flat surface and make sure all sides are at least 1 foot 30 cm away from a wall or other obstruction Do not place the unit in a confined area Choose a dust and smoke free location away from direct sunlight Do not operate the unit outdoors unless the unit is plugged into a Ground Fault Circuit Interrupter GFCI protected outlet CAUTION Do not operate this unit in a restricted or confined space where ventilation can be limited This can cause the device to overheat and affect performance CAUTION Do not allow either the air intake or the air outlet vents to be blocked DO NOT drop or insert any object into any openings on the device This can cause the Oxygen Concentrator to overheat and impair performance CAUTION The Manufacturer recommends an alternate source of supplemental oxygen in the event of a power outage alarm condition or mechanical failure Consult your physician or Equipment Provider for the type of reserve system required CAUTION It is very important to select only the pre scribed l
9. 15 60 Hz 3 0 A Requirements 39 VAC 50 Hz 1 5 230 VAC 60 Hz 1 0 Power VisionAire 2 200 Watts 10 Consumption yiionaire 3 200 Watts 10 Sound 45 dba anechoic Dimensions 14 1 in W x 11 5 in D x 20 8 in H 35 8 cm W x 29 2 cm D x 52 8 cm H Weight 30 Ibs 13 6 kg Electrical Shock Class Il B Protection Environmental Operating conditions 5 C to 40 C 41 F Limit to 104 F at altitudes up to 10 000 ft Conditions 523 mmHg above sea level Storage 20 C to 60 4 F to 140 F Relative Humidity up to 95 RH non condensing 1 10 of indicated setting or 200 mL whichever is greater 2 Performance based at 21 C 70 F at nominal operating pressure range 0 7 kPa 0 1 psig back pressure Maximum outlet pressure 55 kPa 7 98 psig 3 Operating outside of these operational specifications can limit the concentrators ability to meet Oxygen Concentration specification at higher liter flow rates VisionAire 2 amp 3 User Manual 15 visiefiAire Medical equipment needs special precautions regarding EMC and need to be installed and put into service according to the EMC information provided in this section Guidance and Manufacturer s Declaration Electromagnetic Immunity The unit is intended for use in the electromagnetic environment specified below The customer or the user of the unit should assure that it is used in such an environment
10. A CAIRE pedcs VisionAire 2 amp 3 visiefiAire User Controls amp System Status Indicators Definition Read user manual before operation See user manual for instructions No Smoking Icon Do not smoke near unit Warnings and Cautions Type B equipment degree of protection against electric shock Complies with the 93 42 EEC directive drawn up by the approved organization No 0459 CERTIFIED TO CSA SID 22 2 No 601 1 Keep unit and accessories dry Consult the accompanying documents Oxygen outlet connection to the cannula Caution Federal law USA restricts this for sale or rental by or on the order of a physician or licensed health care provider Fragile handle with care Date of Manufacture Serial number Catalog number 2 165 1 Definition ON power switch on OFF power switch off No serviceable parts inside Do not open cover Class equipment Safety agency for CAN CSA C22 2 No 601 1 M90 for medical electrical equipment Use no oil or grease This symbol is to remind the equipment owners to return it to a recycling facility at the end of its life per Waste Electrical and Electronic Equipment WEEE Directive Proper disposal of waste of electrical and electronic equipment required Do not expose to open flames Keep in the vertical position Oxygen concentration warning LED Name and address of manufacturer Authorized r
11. CHAIR CUSHIONS IF THE UNIT IS TURNED ON BUT NOT IN USE THE OXYGEN WILL MAKE THE MATERIAL FLAMMABLE SET THE 1 0 POWER SWITCH TO THE 0 OFF POSITION WHEN THE OXYGEN CONCENTRATOR IS NOT IN USE WARNING USE NO OIL GREASE OR PETROLEUM BASED OR OTHER FLAMMABLE PRODUCTS WITH THE OXY GEN CARRYING ACCESSORIES OR THE OXYGEN CON CENTRATOR ONLY WATER BASED OXYGEN COMPATIBLE LOTIONS OR SALVES SHOULD BE USED OXYGEN ACCELER ATES THE COMBUSTION OF FLAMMABLE SUBSTANCES WARNING CLEAN THE CABINET CONTROL PANEL AND POWER CORD ONLY WITH A MILD HOUSEHOLD CLEANER APPLIED WITH A DAMP CLOTH NOT WET OR SPONGE AND THEN WIPE ALL SURFACES DRY DO NOT ALLOW ANY LIQUID TO GET INSIDE THE DEVICE Note Portable and mobile effect medical electrical e ommunications equipment can ment WARNING DO ATTEMPT ANY MAINTE NANCE OTHER THAN THE POSSIBLE SOLU TIONS LISTED WITHIN THIS MANUAL DO NOT REMOVE COVERS ONLY YOUR EQUIPMENT PROVIDER OR A QUALIFIED SERVICE TECHNICIAN SHOULD REMOVE THE COVERS OR SERVICE THIS DEVICE WARNING ONLY ACCESSORIES RECOMMENDED BY THE MANUFACTURER USE OF ANY OTHER MAY BE HAZARDOUS CAUSE SERIOUS DAMAGE TO YOUR OXYGEN CONCENTRATOR AND WILL VOID THE WARRANTY WARNING THE MANUFACTURER RECOM MENDS AN ALTERNATE SOURCE OF SUPPLE MENTAL OXYGEN IN THE EVENT OF A POWER OUTAGE ALARM CONDITION OR MECHANI CAL FAILURE CONSULT YOUR PHYSICIAN OR EQUIPMENT PROVIDER FOR THE TYPE OF RESERVE SYSTEM REQUIRED WA
12. LIST OF UNDESIRABLE CHEMICAL AGENTS INCLUDES BUT IS NOT LIMITED TO THE FOLLOWING ALCOHOL AND ALCOHOL BASED PRODUCTS CONCENTRATED CHLORINE BASED PRODUCTS ETHYLENE CHLORIDE AND OIL BASED PRODUCTS PINE SOL LESTOILG THESE ARE NOT TO BE USED TO CLEAN THE PLASTIC HOUSING ON THE UNIT AS THEY CAN DAMAGE THE UNIT S PLASTIC WARNING CLEAN THE CABINET CONTROL PANEL AND POWER CORD ONLY WITH A MILD HOUSEHOLD CLEANER APPLIED WITH A DAMP CLOTH OR SPONGE AND THEN WIPE ALL SURFACES DRY DO NOT ALLOW ANY LIQUID TO GET INSIDE THE DEVICE Note Always follow the cannula manufacturer s instructions for proper use Replace the disposable cannula as recom mended by the cannula manufacturer or your Equipment Provider Additional supplies are available from your Equipment Provider Note To prevent a voided AirSep warranty follow all manu facturers instructions Note AirSep does not recommend the sterilization of this equipment Humidifier Bottle optional Check water level daily and add water as needed To clean and disinfect the humidifier follow your Equipment Provider s instructions or the instructions included with the humidifier bottle Outside Cabinet Use a mild household cleaner applied with a damp cloth or sponge to clean the exterior of the concentrator and then wipe all surfaces dry Do not allow any liquids to enter the concentrator VisionAire 2 amp 3 User Manual 13 visiefiAire Troubleshootin
13. P MENT IS PERMITTED WARNING SMOKING WHILE USING OXYGEN IS THE NUMBER ONE CAUSE OF FIRE INJURY AND DEATH YOU MUST FOLLOW THESE SAFETY WARNINGS WARNING DO NOT ALLOW SMOKING CANDLES OR OPEN FLAMES WITHIN THE SAME ROOM OF THE DEVICE OR THE OXYGEN CARRYING ACCESSORIES WARNING SMOKING WHILE WEARING AN OXYGEN CAN NULA CAN CAUSE FACIAL BURNS AND POSSIBLY RESULT IN DEATH WARNING REMOVING THE CANNULA AND PLACING IT ON CLOTHING BEDDING SOFAS OR OTHER CUSHION MATERIAL WILL CAUSE A FLASH FIRE WHEN EXPOSED TO A CIGARETTE HEAT SOURCE SPARK OR OPEN FLAME WARNING IF YOU SMOKE YOU MUST ALWAYS FOLLOW THESE 3 IMPORTANT STEPS FIRST TURN OFF THE OXYGEN CONCENTRATOR TAKE OFF THE CANNULA AND LEAVE THE ROOM WHERE THIS DEVICE IS LOCATED CAUTION Federal USA law restricts this de vice to sale or rental by order of a physician or other licensed health care provider WARNING THIS DEVICE SUPPLIES HIGH CON CENTRATION OXYGEN THAT PROMOTES RAPID BURNING DO NOT ALLOW SMOKING OR OPEN FLAMES WITHIN THE SAME ROOM OF 1 THIS DEVICE OR 2 ANY OXYGEN CARRYING AC CESSORY FAILURE TO OBSERVE THIS WARNING CAN RESULT IN SEVERE FIRE PROPERTY DAMAGE AND OR CAUSE PHYSICAL INJURY OR DEATH WARNING DO NOT USE YOUR OXYGEN CONCENTRATOR IN THE PRESENCE OF FLAMMABLE GASES THIS CAN RESULT IN RAPID BURNING CAUSING PROPERTY DAMAGE BODILY INJURIES OR DEATH WARNING DO NOT LEAVE A NASAL CANNULA ON CLOTH ING BED COVERINGS OR
14. PROXIMIT DE L UNIT D CONNECTER LE CORDON D ALIMENTATION DE LA PRISE LECTRIQUE AVANT DE NETTOYER OU DE FAIRE L ENTRETIEN DE L UNIT AVERTISSEMENT RISQUE DE CHOC LECTRIQUE NE PAS ENLEVER LES COUVERCLES LORSQUE L UNIT EST BRANCH E SEULS VOTRE FOURNISSEUR D QUIPEMENT OU UN TECHNICIEN DE SERVICE QUALIFI DEVRAIT ENLEVER LES COUVERCLES OU FAIRE L ENTRETIEN DE L UNIT WARNING THE OXYGEN CONCENTRATOR SHOULD NOT BE USED ADJACENT TO OR STACKED WITH OTHER EQUIPMENT IF AD JACENT OR STACKED USE IS UNAVOIDABLE THE DEVICE SHOULD BE OBSERVED TO VERIFY NORMAL OPERATION WARNING NO MODIFICATION OF THIS EQUIPMENT IS PERMITTED WARNING USE OF CABLES AND ADAPTERS OTHER THAN THOSE SPECIFIED WITH THE EXCEPTION OF CABLES AND ADAPTERS SOLD BY THE MANUFACTURER OF THE MEDICAL ELECTRICAL EQUIPMENT AS REPLACEMENT PARTS FOR INTERNAL COMPONENTS MAY RESULT IN INCREASED EMISSIONS OF DECREASED IMMUNITY OF THE OXYGEN CONCENTRATOR WARNING USE ONLY ELECTRICAL VOLTAGE AS SPECIFIED ON THE SPECIFICATION LABEL AFFIXED TO THE DEVICE WARNING DO NOT USE EXTENSION CORDS WITH THIS UNIT OR CONNECT TOO MANY PLUGS INTO THE SAME ELECTRICAL OUTLET THE USE OF EXTENSION CORDS COULD ADVERSELY AFFECT THE PERFORMANCE OF THE DEVICE TOO MANY PLUGS INTO ONE OUTLET CAN RESULT IN AN OVERLOAD TO THE ELECTRICAL PANEL CAUSING THE BREAKER FUSE TO ACTIVATE OR FIRE IF THE BREAKER OR FUSE FAILS TO OPERATE 6 MN165 1 H CAUTION Do not position the
15. RNING DO NOT ALLOW EITHER THE AIR INTAKE OR THE AIR OUTLET VENTS TO BECOME BLOCKED DO NOT DROP OR INSERT ANY OBJECTS INTO ANY OPENINGS ON THE DEVICE THIS CAN CAUSE THE OXYGEN CONCENTRA TOR TO OVERHEAT AND IMPAIR PERFORMANCE CAUTION In the event of an alarm or you observe the Oxygen Concentrator is not working properly consult the Troubleshoot ing section in this manual If you cannot resolve the problem consult your Equipment Provider CAUTION To prevent a void warranty follow all manufac turers instructions WARNING ELECTRICAL SHOCK HAZARD TURN OFF THE UNIT AND DISCONNECT THE POWER CORD FROM THE ELECTRIC OUTLET BEFORE YOU CLEAN THE UNIT TO PREVENT ACCIDENTAL ELECTRICAL SHOCK AND BURN HAZARD ONLY YOUR EQUIPMENT PROVIDER OR A QUALIFIED SERVICE TECHNICIAN SHOULD REMOVE THE COVERS OR SERVICE THE UNIT WARNING CARE SHOULD BE TAKEN TO PREVENT THE OXYGEN CONCENTRATOR FROM GETTING WET OR ALLOWING FLUIDS TO ENTER THE UNIT THIS CAN CAUSE THE UNIT TO MALFUNCTION OR SHUT DOWN AND CAUSE AN INCREASED RISK FOR ELECTRICAL SHOCK OR BURNS WARNING DO NOT USE LIQUID DIRECTLY ON THE UNIT A LIST OF UNDESIRABLE CHEMICAL AGENTS INCLUDES BUT IS NOT LIMITED TO THE FOLLOWING ALCOHOL AND ALCOHOL BASED PRODUCTS CONCENTRATED CHLORINE BASED PRODUCTS ETHYLENE CHLORIDE AND OIL BASED PRODUCTS PINE SOLG LESTOILG THESE ARE NOT TO BE USED TO CLEAN THE PLASTIC HOUSING ON THE OXYGEN CONCENTRATOR AS THEY CAN DAMAGE THE UNIT S PLASTIC
16. acturer s safety relief valve is fitted to the warranty compressor outlet and is calibrated to 280 kPa 40 psig idifi 1 Power In the event the unit is operating and TAONIS BE Failure a loss of power occurs an audible Cannula 25 feet 7 6 m 002 4 single pulse intermittent alarm will C 5 Cannula 7 feet 2 1 m CU002 1 C U U activate Humidifier Bottle Tubing TU176 160 Oxygen The oxygen monitor detects any drop U U Monitor in concentration below 82 3 Humidifier Bottle Fitting F0655 1 and activates a visual alarm amber Oxygen Tubing 004 3 LED indicator on front panel If the 25 feet 7 6 m concentration continues to operate below 82 an audible 2 pulse Tubing Cannula Connector CU009 1 intermittent alarm will also activate OxySafe Kit Hi Pressure An over pressure safety feature prevents potential damage to device components at a pressure of 207 Materials in direct or indirect contact kPa 30 psig 2 psig An audible with patient 4 pulse intermittent alarm will activate S62 zh Low An audible 3 pulse intermittent Hig Pressure alarm will activate if the device Impact Polystyrene pressure reduces to lt 35 kPa 5 psig parts psig Gas Outlet Aluminum Black Anodized I psig Nozzle No Flow An obstruction to the flow of On Off Switch DuPont FR50 Warning oxygen such as a pinch or kink in Hour Meter Acrylonitrile But
17. adiene Styrene the delivery cannula will activate an ABS Plastic amp Acrylic audible 6 pulse intermittent alarm ABS STAT TECH AS1000 Product gt 10 micron Filter Circuit Breaker Button Melamine or Urea Formaldehyde Mounting Bushing Polyamide 66 Nylon Cord Strain Nylon Relief Cord Wrap Humidifier Strap Yarn Rubber Humidifier Top Acrylonitrile Butadiene Bottle Styrene ABS Bottle Polypropylene PP Diffuser Polyvinyl Chloride PVC Cannula Polyvinyl Chloride PVC Tubing VisionAire 2 amp 3 User Manual 11 visiefiAire Operating Instructions Review the following information before you operate your oxygen concentrator Note The concentrator releases warm air out the bottom of the unit which can permanently discolor temperature sensi tive flooring surfaces such as vinyl The concentrator should not be used over flooring that is sensitive to heat staining The manufacturer is not responsible for flooring that becomes discolored Humidifier Bottle Connection Optional If additional humidification is required with your oxygen therapy perform the following steps each time you fill or clean the humidifier which may have been initially set up for your use Remove the humidifier bottle from the humidifier bottle recess 2 Open the humidifier bottle If you have a pre filled bottle do not perform this step Proceed to step 5 3 Fill the humidifier bottle with cool
18. d close by such as diathermy and high frequency electro surgical equipment defibrillators short wave therapy equipment mobile telephones CB and other portable devices microwave ovens induction plates or even remote control toys and more generally electromagnetic interferences which exceed the levels specified by the EN 60601 1 2 standard Classification Type of protection against electric shock Class II Protection from electric shock is achieved by DOUBLE INSULATION Protective earthing or reliance upon installation conditions are not required Degree of protection against electric shock Type B Equipment providing a particular degree of protection against electric shock particularly regarding 1 Allowable leakage current 2 Reliability of protective earth connection if present Not intended for direct cardiac application Method of cleaning and infection control allowed Please refer to your Equipment Provider and the VisionAire Service Manual Degree of safety of application in the presence of flammable gases Equipment not suitable for such application Mode of operation Continuous duty VisionAire Disposal Method of disposing of waste All waste from AirSep s VisionAire 2 and VisionAire 3 Oxygen Concentrator must be disposed of using the appropriate methods specified by local authorities Method for disposing of the device In order to preserve the environment the concentrator must be disp
19. epresentative in the European Community Contents User Controls amp System Status Indicators eene 2 Indications for tetuer ame eta ene Rr dinar nra nti maia 4 Contraindications for 0 2222 2 4 Safety Guidelines 22222 4 nippiiapn 8 Concentrator Components essen eene tnn tnter nnn nnns 9 Operating Instructions eeseeseeeeeeeeneeeenn ennt ntn ntn nnn nnne tn ntn tn stant 12 Care eec 13 TROUDISSI O OCING 14 Product Specifications 15 DSP OSal Ic 19 English A multilingual version of the manual is available through your equipment provider Espafiol Una versi n multiling e del manual est disponible a trav s de su proveedor de equipo Francais Une version multilingue du manuel est disponible par l interm diaire de votre fournisseur de mat riel Deutsche Eine mehrsprachige Version des Handbuchs ist in Ihrer Ger te Anbieter VisionAire 2 amp 3 User Manual 3 VisiefiAire Important Safety Instructions are defined as fol lows WARNING IMPORTANT SAFETY INFORMATION FOR HAZARDS THAT MIGHT CAUSE SERIOUS INJURY CAUTION Important information for preventing damage to the VisionAire Note Informatio
20. evel of oxygen Do not change the flow selection unless you have been directed to do so by a licensed clinician CAUTION The Oxygen Concentrator may be used during sleep under the recommendation of a licensed clinician CAUTION Operating or storing the Oxygen Concentrator outside of its normal operating temperature range can impair the performance of the unit Refer to the specifi cation section of this manual for storage and operating temperature limits CAUTION In the event of an alarm or you observe the Oxygen Concentrator is not working properly consult the troubleshooting section of this manual If you cannot resolve the problem consult your Equipment Provider CAUTION If the audio alarm is weak or does not sound at all consult your Equipment Provider immediately CAUTION For units equipped with the oxygen monitor option Contact your Equipment Provider immediately if the amber OXYGEN MONITOR light remains on for more than 15 minutes and or the audio alarm activates CAUTION If the humidifier bottle tubing is not properly connected to the humidifier bottle fitting or to the oxygen outlet an oxygen leak can occur Note Cannula must non kinking which be used for a total length of 25 ft 7 6 m max Note Ensure the cannula is fully inserted and secure You should hear or feel oxygen flow to the prongs of the nasal cannula If oxygen does not seem to flow first verify that the flowmeter ball is regis
21. g If your concentrator fails to operate properly consult your Equipment Provider and refer to the troubleshooting chart on the following pages for probable causes and solutions Note Do not attempt any maintenance other than the possible solutions listed within the manual Vote If the unit has not been used for an extended time period it needs to operate for several minutes before power failure alarm can become activated Unit does The power cord is not Check power cord at the electrical outlet for a proper not operate connected to the electrical connection Powerfailure outlet condition Causes an No power at the electrical Check power source wall switch in house fuse or circuit alarm to outlet breaker sound Circuit breaker on Press do not hold in the circuit breaker reset button in the concentrator unit is front of the unit activated If the circuit breaker trips again or the alarm continues to sound after the unit is turned on contact your Equipment Provider Limited orno Dirty or obstructed Remove the humidifier bottle and if flow is restored clean oxygen flow humidifier bottle or leak or replace the humidifier bottle present Defective nasal cannula or Remove and check accessories for kinks or obstructions other oxygen accessories Replace if needed i e oxygen tubing Cannula tubing loose Check cannula tubing connection at control panel Condensation Unit not properly Make sure unit is p
22. lity descrip tions specifications and or processes to its products at any S time without prior notice and with no further obligation OxySafe is a registered trademark of Applied Home Healthcare Equipment or consequence All rights not expressly stated herein are Pine Sol and Lestoil are registered trademarks of The Clorox Company DD TULIT MN165 1 Rev H
23. n needing special attention Indications for Use WARNING IT IS VERY IMPORTANT TO SELECT ONLY THE PRESCRIBED LEVEL OF OXYGEN DO NOT CHANGE THE FLOW SELECTION UNLESS YOU HAVE BEEN DIRECTED TO DO SO LICENSED CLINICIAN THE PORTABLE OXYGEN CONCENTRA TOR MAY BE USED DURING SLEEP UNDER THE RECOMMEN DATION OF A QUALIFIED CLINICIAN WARNING FEDERAL USA LAW RESTRICTS THIS DEVICE TO SALE OR RENTAL BY ORDER OF A PHYSICIAN OR OTHER LICENSED HEALTH CARE PROVIDER WARNING THIS UNIT IS NOT TO BE USED FOR LIFE SUPPORT GERIATRIC PEDIATRIC OR ANY OTHER PATIENT UNABLE TO COMMUNICATE DISCOMFORT WHILE USING THIS DEVICE MAY REQUIRE ADDITIONAL MONITORING PATIENTS WITH HEARING AND OR SIGHT IMPAIRMENT S MAY NEED ASSISTANCE WITH MONITORING ALARMS Contraindications for Use WARNING IN CERTAIN CIRCUMSTANCES THE USE OF NON PRESCRIBED OXYGEN CAN BE HAZARDOUS THIS DEVICE SHOULD ONLY BE USED WHEN PRESCRIBED BY A PHYSICIAN WARNING NOT FOR USE IN THE PRESENCE OF FLAMMABLE ANESTHETICS WARNING AS WITH ANY ELECTRICALLY POWERED DEVICE THE USER MAY EXPERIENCE PERIODS OF NON OPERATION AS A RESULT OF ELECTRICAL POWER INTERRUPTION OR THE NEED TO HAVE THE VISIONAIRE SERVICED BY A QUAL IFIED TECHNICIAN THE VISIONAIRE IS NOT APPROPRIATE FOR ANY PATIENT WHO WOULD EXPERIENCE ADVERSE HEALTH CONSEQUENCES AS THE RESULT OF SUCH TEMPO RARY INTERRUPTION 4 MN165 1H Safety Guidelines WARNING NO MODIFICATION OF THIS EQUI
24. ny interference in nearby electronic equipment RF emissions Class B CISPR 11 Harmonic emissions Class A The unit is suitable for use in all establishments including domestic es IEC 61000 3 2 ass tablishments and those directly connected to the public low voltage pow er supply network that supplies buildings used for domestic purposes Voltage fluctuations flicker emissions Complies IEC 61000 3 3 18 165 1 Conformity with 60 601 8 6 8 2 b Classification manufacturer assembler installer or importer are not considered to be responsible themselves for the consequences on the safety reliability and characteristics of a device unless The assembly fitting extensions adjustments modifications or repairs have been performed by persons authorized by the party in question The electrical installation of the corresponding premises complies with IEC regulations The device is used in accordance with the instructions for use If the replacement parts used for the periodic servicing by an approved technician do not comply with the manufacturer s specifications the latter is absolved from all responsibility in the event of an accident Do not open the device while in operation risk of electrical shock This device complies with the requirements of the MDD 93 42 EEC 2007 47 EC Annex I European directive but its operation may be affected by other devices being use
25. ords in a manner that prevents a trip hazard WARNING THE OXYGEN CONCENTRATOR SHOULD NOT BE USED ADJACENT TO OR STACKED WITH OTHER EQUIPMENT IF AD JACENT OR STACKED USE IS UNAVOIDABLE THE DEVICE SHOULD BE OBSERVED TO VERIFY NORMAL OPERATION WARNING NO MODIFICATION OF THIS EQUIPMENT IS PERMITTED WARNING USE OF CABLES AND ADAPTERS OTHER THAN THOSE SPECIFIED WITH THE EXCEPTION OF CABLES AND ADAPTERS SOLD BY THE MANUFACTURER OF THE MEDICAL ELECTRICAL EQUIPMENT AS REPLACEMENT PARTS FOR INTERNAL COMPONENTS MAY RESULT IN INCREASED EMISSIONS OF DECREASED IMMUNITY OF THE OXYGEN CONCENTRATOR WARNING USE ONLY ELECTRICAL VOLTAGE AS SPECIFIED ON THE SPECIFICATION LABEL AFFIXED TO THE DEVICE WARNING DO NOT USE EXTENSION CORDS WITH THIS UNIT OR CONNECT TOO MANY PLUGS INTO THE SAME ELECTRICAL OUTLET THE USE OF EXTENSION CORDS COULD ADVERSELY AFFECT THE PERFORMANCE OF THE DEVICE TOO MANY PLUGS INTO ONE OUTLET CAN RESULT IN AN OVERLOAD TO THE ELECTRICAL PANEL CAUSING THE BREAKER FUSE TO ACTIVATE OR FIRE IF THE BREAKER OR FUSE FAILS TO OPERATE VisionAire 2 amp 3 User Manual 5 visiefiAire AVERTISSEMENT CET APPAREIL PRODUIT DE A CONCENTRATION LEV E FAVORISANT UNE COMBUSTION RAPIDE NE PAS PERMETTRE DE FUMER OU DES FLAMMES NUES DANS LA M ME CHAMBRE 1 CET APPAREIL OU 2 TOUT ACCESSOIRE CONTENANT DE L OXYGENE NE PAS UTILISER DE PRODUITS BASE D HUILE DE GRAISSE OU DE P TROLE SUR OU
26. osed of using the appropriate methods specified by local authorities AVERTISSEMENT CET APPAREIL PRODUIT DE A CONCENTRATION LEV E FAVORISANT UNE COMBUSTION RAPIDE NE PAS PERMETTRE DE FUMER OU DES FLAMMES NUES DANS LA MEME CHAMBRE 1 CET APPAREIL OU 2 TOUT ACCESSOIRE CONTENANT DE L OX NE PAS UTILISER DE PRODUITS BASE D HUILE DE GRAISSE OU DE P TROLE SUR OU PROXIMIT DE L UNIT D CONNECTER LE CORDON D ALIMENTATION DE LA PRISE LECTRIQUE AVANT DE NETTOYER OU DE FAIRE L ENTRETIEN DE L UNIT AVERTISSEMENT RISQUE DE CHOC LECTRIQUE NE PAS ENLEVER LES COUVERCLES LORSQUE L UNIT EST BRANCH E SEULS VOTRE FOURNISSEUR D QUIPEMENT OU UN TECHNICIEN DE SERVICE QUALIFI DEVRAIT ENLEVER LES COUVERCLES OU FAIRE L ENTRETIEN DE L UNIT VisionAire 2 amp 3 User Manual 19 VisiohAire cal AirSep 260 Creekside Drive Buffalo NY 14228 2075 USA 1 800 482 2473 Worldwide www CAlREmedical com Medical Product Services GmbH Borngasse 20 35619 Braunfels Germany Worldwide www CAlREmedical com 4 0459 277 Chart Industries Company AirSep As of the date of this publication VisionAire AirSep and their related logos as applicable are trademarks registered by CAIRE Inc CAIRE Inc reserves the right to discontinue its products or Lysol is a registered trademark of Reckitt Benckiser UK change the prices materials equipment qua
27. ositioned away from curtains or drapes collects in the ventilated hot air registers or heaters Be certain to place the unit so all oxygen tubing Elevated operating sides are at least 1 foot 30 cm away from a wall or other when you use temperatures obstruction Do not place the unit in a confined area a humidifier Refill humidifier bottle with COLD water bottle DO OVERFILL Allow oxygen tubing to dry out or replace with new tubing Intermittent See Safety Features for Set 1 0 power switch to 0 position use your reserve oxygen alarm sounds a description of auditory supply if provided and consult your Equipment Provider atonesecond indicators immediately intervals Oxygen Oxygen concentration is lt Set 1 0 power switch to the 0 position use your reserve Concentration 82 3 oxygen supply if provided and consult your Equipment Indicator Provider immediately remains lit amber All other Set 1 0 power switch to the 0 position use your reserve problems oxygen supply if provided and consult your Equipment Provider immediately 14 165 1 VisionAire Product Specifications For correct use of the device refer to the following chart The chart provides important information about the recommended operating environments or operating conditions Specifications Flow 1 2 3 Specifications 1 8 pm 2 Ipm Oxygen 90 5 5 3 Concentration Electrical 1
28. revent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the unit as recommended below according to the maximum output power of the communications equipment Rated maximum Separation distance according to frequency of transmitter output power of m transmitter 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2 5 GHz For transmitters rated at a maximum output power not listed above the recommended separation distance d in metres m can be estimated using the equation applicable to the frequency of the transmitter where P is the maxi mum output power rating of the transmitter in watts W according to the transmitter manufacturer NOTE 1 At 80 MHz and 800 MHz the separation distance for the higher frequency range applies NOTE 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people Guidance and Manufacturer s Declaration Electromagnetic Emissions The unit is intended for use in the electromagnetic environment specified below The customer or the user of the unit should assure that it is used in such an environment Emissions Test Compliance Electromagnetic Environment Guidance RF emissions The unit uses RF energy only for its internal function Therefore its RF Group 1 emissions are very low not likely to cause a
29. ring power mains interruptions it is recommended that the unit be powered from an uninterrupt ible power supply or a battery Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment NOTE U is the A C mains voltage prior to application of the test level 16 MN165 1 H VisiohAire Guidance and Manufacturer s Declaration Electromagnetic Immunity The unit is intended for use in the electromagnetic environment specified below The customer or the user of the unit should assure that it is used in such an environment Immunity test IEC 60601 test Compliance Electromagnetic environment guidance level level Conducted RF 3 Vrms Portable and mobile RF communications equipment IEC 61000 4 6 150 kHz to 80 should be used no closer to any part of the VisionAire MHz including cables than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter Radiated RF IEC 61000 4 3 3 V m Recommended separation distance 80 MHz to 2 5 GHz d 12 d 1 2 P 80 MHz to 800 MHz d 800 MHz to 2 5 GHz Where P is the maximum output power rating of the transmitter in watts W according to the transmitter manufacturer and d is the recommended separation distance in metres m Field strengths from fixed RF transmitters as deter mined by an electromagnetic site survey should be less
30. sensi tive flooring surfaces such as vinyl The concentrator should not be used over flooring that is sensitive to heat staining The Manufacturer is not responsible for flooring that becomes discolored Note To prevent a void warranty follow all manufacturers instructions Note Do not attempt any maintenance other than the possi ble solutions listed within the manual Note Portable and mobile RF communications equipment can effect medical electrical equipment Note There is never a danger of depleting the oxygen in a room when you use your Oxygen Concentrator unit VisionAire Note AirSep offers the OxySafe as an optional accessory This is intended to be used in conjunction with the Visionaire 2 3 concentrator For customers in regions requiring compliance to EN ISO 8359 1996 Ammendment1 2012 this accessory will meet this need The OxySafe is a thermal fuse to stop the flow of gas in the event that the downstream cannula or oxygen tubing is ignited and burns to the OxySafe It is placed in line with the nasal cannula or oxygen tubing between the patient and the oxygen outlet of the Visionaire 2 3 For proper use of the OxySafe always refer to the manufac turer s instructions included with each OxySafe kit AirSep offers an OxySafe kit that includes OxySafe with 2 of tubing to connect to the oxygen outlet PN 20629671 VisionAire 2 amp 3 User Manual 7 visiefiAire Introduction This Patient Man
31. tering a flow Then place the tip of the cannula into a glass of water if bubbles come out of the cannula oxygen is flowing If bubbles do not appear refer to the troubleshooting section of this manual Note Always follow the cannula manufacturer s instructions for proper use Replace the disposable cannula as recom mended by the cannula manufacturer or your Equipment Provider Additional supplies are available from your Equipment Provider Note The use of some oxygen administration accessories not specified for use with this oxygen concentrator may impair its performance Recommended accessories are referenced within this manual Note To Equipment Provider The following oxygen adminis tration accessories are recommended for use with the Oxygen Concentrator Humidifier Bottle Part No HU003 1 Nasal Cannula with 7 feet 2 1 m of tubing Part No CU002 1 OxySafe Kit Part No 20629671 Note The Manufacturer does not recommend the sterilization of this equipment Vote If the unit has not been used for an extended time period it needs to operate for a minimum of several minutes before power failure alarm can become activated Note For units equipped with the oxygen monitor option When you turn the unit on it s normal for the amber OXYGEN MONITOR light to turn on and remain on for up to five minutes Vote The concentrator releases warm air out the bottom of the unit which can permanently discolor temperature
32. u have been directed to do so by a licensed clinician Normally you should not need to adjust the flowmeter on your unit If you turn the flowmeter adjustment knob clockwise you will decrease and can shut off the flow of oxygen from your unit Note Ensure the cannula is fully inserted and secure You should hear or feel oxygen flow to the prongs of the nasal cannula If oxygen does not seem to flow first verify that the flowmeter ball is registering a flow Then place the tip of the cannula into a glass of water if bubbles come out of the cannula oxygen is flowing If bubbles do not appear refer to the troubleshooting section of this manual CAUTION Ensure concentrator is operated in an upright position Turning the Concentrator Off Set the I 0 power switch to the 0 position to turn off the unit visiefiAire Care and Cleaning WARNING ELECTRICAL SHOCK HAZARD TURN OFF THE UNIT AND DISCONNECT THE POWER CORD FROM THE ELECTRIC OUTLET BEFORE YOU CLEAN THE UNIT TO PREVENT ACCIDENTAL ELECTRICAL SHOCK AND BURN HAZARD ONLY YOUR EQUIPMENT PROVIDER OR A QUALIFIED SERVICE TECHNICIAN SHOULD REMOVE THE COVERS OR SERVICE THE UNIT WARNING CARE SHOULD BE TAKEN TO PREVENT THE OXYGEN CONCENTRATOR FROM GETTING WET OR ALLOWING FLUIDS TO ENTER THE UNIT THIS CAN CAUSE THE UNIT TO MALFUNCTION OR SHUT DOWN AND CAUSE AN INCREASED RISK FOR ELECTRICAL SHOCK OR BURNS WARNING DO NOT USE LIQUID DIRECTLY ON THE UNIT A
33. ual will acquaint you with AirSep s VisionAire 2 and VisionAire 3 Oxygen Concentrators Make sure you read and understand all of the information contained in this guide before operating your concentrator Should you have any questions your Equipment Provider will be happy to answer them for you Why Your Physician Prescribed Oxygen Many people today suffer from a variety of heart lung and other respiratory diseases A significant number of these patients can benefit from supplemental oxygen therapy for respiratory care at home in the hospital or at a medical facility Oxygen is a gas that makes up 21 of the room air we breathe Our bodies depend on a steady supply to function properly Your physician has prescribed supplemental oxygen therapy because your body is not able to get enough oxygen from room air Oxygen is a non addictive drug and your physician prescribed a flow sufficient to improve your condition Please keep in mind that unauthorized oxygen therapy can be dangerous You must seek medical advice before you use this unit The Equipment Provider who supplies your oxygen equipment will demonstrate how to set the prescribed flow rate What is an Oxygen Concentrator Oxygen concentrators were introduced in the mid 1970s and have become the most convenient reliable source of supplemental oxygen available today Without an oxygen concentrator the average patient would require a delivery of 12 bottles cylinders of o
34. xygen each month Your oxygen concentrator produces all the oxygen you need with no deliveries required The air we breathe contains approximately 21 oxygen 78 nitrogen and 1 other gases In the VisionAire 2 or VisionAire 3 unit room air passes through a regenerative adsorbent material called molecular sieve This material separates the oxygen from the nitrogen and other gases The result is a constant supply of high concentration supplemental oxygen that is delivered to the patient Note There is never a danger of depleting the oxygen in a room when you use your VisionAire 2 or VisionAire 3 unit 8 165 1 Operator Profile AirSep s Stationary Concentrators are intended to supply supplemental Oxygen to users suffering from discomfort due to ailments which affect the efficiency of ones lungs to transfer the oxygen in air to their bloodstream Users can benefit from supplemental oxygen therapy for respiratory care at home in the hospital or at a medical facility Oxygen Concentrator use requires a physician s prescription and are not intended for life support use Although Oxygen therapy can be prescribed for patients of all ages the typical oxygen therapy patient is older than 65 years of age and suffers from chronic obstructive pulmonary disease COPD Patients typically have good cognitive abilities and must be able to communicate discomfort If the user is unable to communicate discomfort or unable to read
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