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2 - ENG    PN MN239 F | User Manual

NewLife Intensity 10

User Controls & System Status Indicators

ISO 7000; Graphical symbols for use on  

equipment—Index and synopsis

Read user’s manual before operation. 

Reg. # 1641

Storage or operating temperature 

range. Reg. # 0632

Storage humidity range. Reg. # 2620

Atmospheric pressure limitation. Reg. 

# 2621

Keep away from rain, keep dry. Reg. 

# 0626

Name and address of manufacturer. 

Reg. # 3082

 

 

Caution, consult accompanying docu-

ments. Reg. # 0434A

Catalog Number. Reg. # 2493

Serial Number. Reg. # 2498

This way up. Reg. # 0623

Fragile, handle with care. Reg. # 

0621
Stacking limit by number. Reg. # 

2403

ISO 7010: Graphical symbols—Safety colors and 

safety signs—Registered safety signs

The instruction manual must be read. 

Reg. # M002

Keep away from open flame, fire, 

sparks. Open ignition source and 

smoking prohibited. Reg. # P003

Do not smoke near unit or while 

operating unit. Reg. # P002

Type BF applied part (degree of 

protection against electric shock). 

Reg. # 5333

Warning. Reg. # W001

Council Directive 93/42/EEC; concerning  

medical devices

Authorized representative in the 

European Community

If the product unique device identifier 

(UDI) label has the CE#### symbol 

on it, the device complies with the 

requirements of Directive 93/42/EEC 

concerning medical devices. The 

CE#### symbol indicates notified 

body number.

Internal Symbols

Keep away from flammable materials, 

oil and grease.

Safety agency for CAN/CSA 

C22.2 No. 60601-1-14 for medical 

electrical equipment. Certified for 

both the U.S. and Canadian markets, 

to the applicable U.S. and Canadian 

standards. 

Do not disassemble.

When present on the device alarm 

panel indicates external power inter-

ruption has been detected.
When present on the device alarm 

panel indicates low oxygen concen-

tration in device output.

ON (power switch on)

OFF (power switch off)

Date of Manufacture

Class II equipment

21 CFR 801.15: Code of Federal Regulations Title 

21

Federal law restricts this device to 

sale by or on the order of a physician.

Summary of Contents for NewLife Intensity 10

Page 1: ...NewLife Intensity 10 User Manual English...

Page 2: ...Type BF applied part degree of protection against electric shock Reg 5333 Warning Reg W001 Council Directive 93 42 EEC concerning medical devices Authorized representative in the European Community I...

Page 3: ...home when traveling or while participating in daily activities away from home Oxygen is a gas that makes up 21 of the room air we breathe Our bodies depend on a steady supply to function properly You...

Page 4: ...n operate at any location where AC power source is available Oxygen concentrator use requires a physician s prescription and is not intended for life support use Although oxygen therapy can be prescri...

Page 5: ...perating Instructions Explains procedures to operate the unit H Air Intake Gross Particle Filter Prevents dust and other airborne particles from entering the unit I Power Cord Allows connection of uni...

Page 6: ...RDOUS 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 EXPERIENC...

Page 7: ...ntal by order of a physician or other licensed health care provider CAUTION Do not position the unit so that it is difficult to access the power cord CAUTION The concentrator should be located as to a...

Page 8: ...m capacity of the concentrator Note To prevent a void warranty follow all manufac turers instructions Note Do not attempt any maintenance other than the possible solutions listed within the manual Not...

Page 9: ...Pressure 20 psig 138 kPA Operating Environment 41 F to 104 F 5 C to 40 C 15 90 humidity Altitude 1250 to 10 000 ft 381 to 3048 m tested to 700 1060 hPa Storage Environment 25 C to 70 C 13 F to 158 F...

Page 10: ...if required nasal cannula face mask catheter and or extension tubing to the oxygen outlet 5 Completely unwrap the power cord 6 Insert power cord into the electrical outlet 7 Locate the power switch on...

Page 11: ...BE USED OXYGEN AC CELERATES THE COMBUSTION OF FLAMMABLE SUBSTANCES WARNING THE USE OF SOME OXYGEN ADMIN ISTRATION ACCESSORIES NOT SPECIFIED FOR USE WITH THIS OXYGEN CONCENTRATOR MAY IMPAIR ITS PERFOR...

Page 12: ...If your physician did not prescribe a humidi fier connect the oxygen tubing directly to the unit s oxygen outlet A separate outlet fitting is supplied for this type of connection Operating With Humidi...

Page 13: ...pter or humidifier Note To Equipment Provider The following oxygen administration accessories are recommended for use with the NewLife Oxygen Concentrator Nasal Cannula with 7 feet 2 1 m of tubing 6 L...

Page 14: ...ermal switch located within the compressor trips shutting down the compressor Oxygen Monitor In the event the oxygen monitor detects an oxygen concentration below 82 the low oxygen concentration warni...

Page 15: ...cation as prescribed by your physician Note Use only the amount of medication and frequen cy of treatment that your physician prescribed 3 Remove or unscrew the medication cup on the nebulizer and pl...

Page 16: ...er parts 1 After each treatment separate the nebulizer and the T piece or mouthpiece assembly 2 Remove or unscrew the nebulizer cup and rinse each component thoroughly in warm water 3 Once a day clean...

Page 17: ...ICAL 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 EQUIP MENT PROVIDE...

Page 18: ...least one time each week wash the air intake gross particle filter which is located in the back of the unit Your Equipment Provider may advise you to clean it more often depending upon your operating...

Page 19: ...d intermittent audible alarm Power Failure Ensure device is plugged into a known working outlet Ensure breaker switch is pushed in If issue persists contact equipment provider for service Troubleshoot...

Page 20: ...e unit is positioned away from curtains or drapes hot air registers heaters and fireplac es Be certain to place the unit so all sides are at least 12 inches 30 5 cm away from a wall or other obstructi...

Page 21: ...ard Accessories Nasal Cannula with 7 feet 2 1 m of tubing 6 LPM max CU002 1 Oxygen Outlet Adapter F0025 1 Face Mask with 7 feet 2 1 m of tubing 10 LPM max MS013 1 Humidifier Adapter Extension HU002 1...

Page 22: ...ed in such an environment Emissions Test Compliance Electromagnetic Environment Guidance RF emissions CISPR 11 Group 1 The NewLife uses RF energy only for its internal function There fore its RF emiss...

Page 23: ...l on AC lines 2kV common mode on outdoor I O lines N A 1kV differential on AC lines N A Mains power quality should be that of a typical commercial or hospital environment Voltage dips short interrupti...

Page 24: ...lectromag netic site survey a should be less than the compliance level in each frequency range b Interference may occur in the vicinity of equipment marked with the following symbol NOTE 1 At 80 MHz a...

Page 25: ...distance between the transmitting antenna and the ME EQUIPMENT OR ME SYSTEM may be reduced to 1m The 1 m test distance is permitted by IEC 61000 4 3 a For some services only uplink frequencies are in...

Page 26: ...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 i...

Page 27: ...PN MN239 F User Manual ENG 27 NewLife Intensity 10 Notes...

Page 28: ...IRE Inc Please visit our website below for a full listing of trademarks Trademarks www caireinc com corporate trademarks Copyright 2022 CAIRE Inc All Rights Reserved CAIRE Inc reserves the right to di...

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