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AIROS AIROS 8, Руководство по эксплуатации

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23

A8IFU.0001 REV C

Guidance and Manufacturer’s 

Declaration – Electromagnetic 

Immunity

1.  The AIROS 8 Sequential Compression Device needs special precautions 

regarding EMC and needs to be installed and put into service according to 

EMC information provided in the Operating Instructions.  

2.  Portable and mobile RF communications equipment can affect the AIROS 8 

Sequential Compression Device.

 
Technical Description

CAUTION

: 

The use of accessories, transducers, and cables other 

than those specified with the exception of transducers and cables 

sold by the manufacturer of the AIROS 8 Sequential Compression 

Device as replacement parts for internal components, may result 

in increased EMISSIONS or decreased IMMUNITY of the AIROS 8 

Sequential Compression Device.  

 

CAUTION: 

The AIROS 8 Sequential Compression Device should not 

be used adjacent to or stacked with other equipment. 

Содержание AIROS 8

Страница 1: ...OPERATING INSTRUCTIONS FOR USE GUIDE AIROS 8 Sequential Compression Device www airosmedical com 1 866 991 6956...

Страница 2: ......

Страница 3: ...ton Functions 5 Front Panel Display Overview 5 Back Panel Power Switch Fuse Plug 6 Garment Overview 7 Device Operation Specifications 8 Operating Instructions 9 Troubleshooting 18 Error Messages Alarm...

Страница 4: ...ome and hospital use Contraindications Pneumatic compression IS NOT recommended for use in patients with the following conditions Infections in the limb including cellulitis without appropriate antibi...

Страница 5: ...Electrical Shock Hazard Disconnect Line Cord before servicing Refer servicing to a qualified service representative Class II Equipment Protected against solid foreign objects of 12 5mm and greater Pr...

Страница 6: ...lectrical Shock Class II Operation Mode CONTINUOUS Protection Against Water IP21 TEMPERATURE Operating Temperature 41 F 5 C 104 F 40 C Storage Temperature 13 F 25 C 158 F 70 C Transportation Temperatu...

Страница 7: ...ular fluid clearance The AIROS 8 system consists of the device and 8 chambered garments The device provides cycles of compressed air at certain adjustable pressures and sequentially inflates the garme...

Страница 8: ...real time device information LCD Specification 5 volts DC max 0 5 amp 4 lines x 20 characters per line presentation Status Indication Green LED Indicates that treatment is being administered Yellow LE...

Страница 9: ...OWER SWITCH Power can be turned on or off FUSE One 1 time delayed fuse inside for protection against electrical short circuit POWER PLUG Power source Device Panels Back Panel MAIN POWER SWITCH POWER P...

Страница 10: ...ssue is forced towards the gap causing a creased area with restricted blood flow The design of the garments ensures high patient comfort 8 CHAMBER GARMENT TUBES GARMENT CONNECTOR 8 Chamber Garment App...

Страница 11: ...e Gradient Mode operation with 45mmHg of pressure in the distal chamber a 60 minute therapy time a 60 second cycle time Lymphedema Preparation Treatment LPT Mode set to OFF and no chambers skipped PRI...

Страница 12: ...sure Mode therapy Operating Instructions 1 Unpacking the Equipment 1 1 Open the shipping box and remove the device 1 2 Remove the protective foams and bag 1 3 Remove the garments from the bag 1 4 Unro...

Страница 13: ...m through the internal part of the garment CAUTION The detachable power supply cord may pose a risk of strangulation 3 Treatment Therapy NOTE Device settings can only be modified or restored before or...

Страница 14: ...To change the number of sleeves for treatment the user must reset the device to Factory Default settings Refer to the instructions in 3 10 Press the UP or DOWN buttons to move the arrow on the screen...

Страница 15: ...hanged and is fixed at 4 To set the Pressure press UP or DOWN to scroll to PRESSURE Press SELECT to confirm The pressure will begin blinking Press UP or DOWN to scroll from 30 80 mmHg in increments of...

Страница 16: ...scroll to LPT MODE Press SELECT to confirm The LPT Mode option will begin blinking Press UP or DOWN to scroll through the settings including OFF CLEARING and FOCAL If you select FOCAL THERAPY proceed...

Страница 17: ...to confirm The pressure will begin blinking Press UP or DOWN to choose from 10 or 15 minutes Press SELECT to confirm The pressure will be updated and stop blinking To exit and return to a therapy mod...

Страница 18: ...LECT to confirm The therapy time will begin blinking Press UP or DOWN to scroll to 15 30 45 or 60 minutes Press SELECT to confirm The cycle time will be updated and stop blinking To select a chamber i...

Страница 19: ...al instructions If this is not the first time the device is being used you may not be asked to select the number of sleeves Treatment will begin immediately 3 9 USAGE DATA SCREEN This screen shows the...

Страница 20: ...YES Press SELECT to confirm The device will run another deflation session for five minutes 300 seconds At the end of this deflation session the START UP SCREEN will appear 4 4 If you do not need to ru...

Страница 21: ...Keep away from explosive or flammable anesthetic gas Troubleshooting Error Messages Alarms High Pressure This can occur if there is a kink or other obstruction in the tubing connecting the garments or...

Страница 22: ...e device Fuse Replacement The safety fuse on the back panel of the device can sometimes blow for different reasons such as a power surge or the normal aging of the electronic components The safety fus...

Страница 23: ...OTE DO NOT use abrasive materials such as a scrubbing pad cleaning chemicals or detergents containing bleach as they may cause damage to the garment NOTE If directed methods for cleaning the garments...

Страница 24: ...Limited Warranty shall be at its sole discretion to repair or replace a Device that is defective in either workmanship or material This is the sole remedy of the Purchaser In addition this Limited War...

Страница 25: ...st ingress of water According to the degree of protection against harmful ingress of water this system is classified as Ordinary Equipment IP21 Protected against solid foreign objects of 12 5mm and gr...

Страница 26: ...t can affect the AIROS 8 Sequential Compression Device Technical Description CAUTION The use of accessories transducers and cables other than those specified with the exception of transducers and cabl...

Страница 27: ...p 1 The AIROS 8 Sequential Compression Device uses RF energy only for its internal function Therefore its RF emissions are very low and are not likely to cause any interference in nearby electronic eq...

Страница 28: ...ne s and neutral 1 kV line s and neutral Mains power quality should be that of a typical commercial or hospital environment Voltage dips short interruptions and voltage variations on power supply inpu...

Страница 29: ...re orienting or relocating the AIROS 8 Sequential Compression Device Immunity test IEC 60601 test level Compliance level Electromagnetic Environment Guidance Conducted RF IEC 6100 4 6 3 Vrms 150 kHz...

Страница 30: ...t power of the communications equipment For transmitters rated at a maximum output power not listed above the recommended separation of distance d in meters m can be estimated using the equation appli...

Страница 31: ...28 N O T E S...

Страница 32: ...www airosmedical com 1 866 991 6956...

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