AIROS AIROS 8 Operating Instructions For Use Manual Download Page 14

11

A8IFU.0001 REV C

Operating Instructions (continued)

3.1

START-UP SCREEN

Press the MAIN POWER SWITCH located on the Rear Panel 

of the device to the “ON” position. The device’s screen will 

illuminate. The START-UP SCREEN will appear.

To use the device for the first time and begin treatment 

immediately with Factory Default settings, press the 

orange START|STOP BUTTON. Proceed to 3.2 for further 

instructions to begin treatment.

If the device has been used before, press the orange 

START|STOP BUTTON. Treatment will begin immediately 

using settings that have been programmed previously.

To view or change settings before treatment, access the 

MAIN MENU SCREEN by pressing and holding down the 

SELECT BUTTON for 5 seconds. Proceed to 3.3.

3.2

START-UP SCREEN

NOTE: After selecting the number of sleeves for treatment 

the first time, the device will remember this selection. The 

user will not need to select the number of sleeves the next 

time they operate the device. 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 next to “1 Sleeve” for unilateral treatment with 

one leg or arm, or “2 Sleeves” for bilateral treatment with 

two legs or arms. Press the SELECT button to confirm your 

selection.

Treatment will begin immediately.    

3.3

MAIN MENU SCREEN

This is the MAIN MENU SCREEN

To select your therapy mode and adjust settings, press UP 

 DOWN 

 to scroll to THERAPY MODES. Press SELECT 

to confirm and proceed to 3.4

To view usage data, press UP 

 

or DOWN 

 to scroll to 

USAGE DATA. Press SELECT to confirm and proceed to 3.9.

To reset the settings on the device to Factory Default 

settings, press UP 

 

or DOWN 

 to scroll to RESET TO 

DEFAULT. Press SELECT to confirm and proceed to 3.10.

To begin treatment therapy, press UP 

 

or DOWN 

 to 

scroll to BEGIN TREATMENT. Refer to 3.2 for additional 

instructions to begin treatment.

AIROS MODEL 8

PRESS START/STOP TO

BEGIN TREATMENT NOW

SELECT # OF SLEEVES 

FOR USE IN TREATMENT 

 

1 SLEEVE

     2 SLEEVES

 

THERAPY MODES

  USAGE DATA

  RESET TO DEFAULT
  BEGIN TREATMENT

Summary of Contents for AIROS 8

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

Page 2: ......

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 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...

Page 31: ...28 N O T E S...

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

Reviews: