Indications for Use The AIROS 6 Sequential Compression Device utilizes gradient pneumatic compression, which is intended for treatment of patients with the following conditions: • Lymphedema • Venous stasis ulcers • Venous insufficiency • Peripheral edema The device is safe for both home and hospital use.
Overview & Description of Symbols NOTE: Refer to Accompanying Documents for more information regarding the system use or description. Type BF - Applied Part Dangerous Voltage – 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 Ø...
General Equipment Specifications 10.2” W x 10.5” D x 4.3” H Dimension (260 mm W x 267 mm D x 110 mm H) 6.4 lbs. (2.88 kg) Weight User Set Inflation 12 Seconds Deflation User Set Cycle Time 120 VAC, 60 Hz, 100VA MAX Electrical 2.5 AMP T250VACH SLO-BLO Fuse Rated...
The application of gradient sequential compression increases blood flow and encourages extracellular fluid clearance. The AIROS 6 system consists of the device and 6-chambered garments. The device provides cycles of compressed air and sequentially inflates the garments from distal to proximal.
Device Panels: Front Panel UP B UTTON LCD SCRE E N START|STOP BUTTON D OW N BU TTON STATUS LED LIG HTS SE LE CT BUT TO N GARME NT CO NNECTOR PORTS Button Functions Status Indication • START|STOP BUTTON: Allows •...
Device Panels: Back Panel MAIN PO WE R SW ITCH P O WE R PLUG FUSE • MAIN POWER SWITCH: Power can be turned on or off. • FUSE: One (1) time-delayed fuse inside for protection against electrical short circuit. POWER PLUG: •...
6-Chamber Garment The segments within the garments are constructed to prevent ‘ridging.’ (Ridging occurs if there is a gap between two compressed areas of tissue. Tissue is forced towards the gap causing a creased area with restricted blood flow.) The design of the garments ensures high patient comfort. •...
Therapy Time Primary Operating Mode The primary operating mode in which the AIROS 6 can be used is Gradient Mode. The user can set the starting pressure in Chamber 1 on the garment, the most distal chamber. Pressure decreases at a fixed gradient of 5% moving distally to proximally.
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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. Unroll the tubes and unroll the garment by spreading it out flat. 2.
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Operating Instructions (continued) Press the MAIN POWER SWITCH located on the Rear Panel START-UP SCREEN of the device to the “ON” position. The device’s screen will illuminate. The START-UP SCREEN will appear. AIROS MODEL 6 To use the device for the first time and begin treatment PRESS START/STOP TO immediately with Factory Default settings, press the BEGIN TREATMENT NOW...
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Operating Instructions (continued) NOTE: Press UP or DOWN to scroll to MORE or GRADIENT MODE SET-UP PREVIOUS to view additional settings options. SCREEN The gradient cannot be changed and is fixed at 5%. GRADIENT: 5% To set the Pressure, press UP or DOWN to scroll to PRESSURE: 45mmHg ...
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Operating Instructions (continued) To set the Pressure, press UP or DOWN to scroll to FOCAL THERAPY MODE PRESSURE. Press SELECT to confirm. The pressure will SET-UP SCREEN begin blinking. Press UP or DOWN to choose from 40, 45, or 50 mmHg.
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Operating Instructions (continued) This screen shows the amount of total time the device has USAGE DATA SCREEN been in used. TOTAL USAGE TIME To go back to the MAIN MENU SCREEN, press UP or HOURS: 0 DOWN to scroll to BACK TO MAIN MENU. Press SELECT MINUTES: 0 to confirm.
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Operating Instructions (continued) 4. End of Therapy 4.1. Therapy will end after the treatment time has elapsed. The user can also stop therapy at any time during a treatment session by pressing the START|STOP BUTTON 4.2. When therapy is ended, the device will vacuum air out of the garment for three minutes (180 seconds).
The LCD screen will read E03, the red LED light will illuminate, and an alarm will sound. NOTE: If you receive any of these error messages, press the START|STOP BUTTON, which will begin deflation of the garments. Then, contact your local authorized dealer or AIROS Medical. A6IFU.0001 REV C...
NOTE: The outer safety fuse is the only item serviceable by someone other than an AIROS Medical trained technician. AIROS Medical trained technicians have been trained specifically for the manufacture...
NOTE: If directed methods for cleaning the garments do not remove all soiling, discard the garments and contact AIROS Medical or an authorized AIROS Medical dealer to obtain new garments. Garment Sizes Contact AIROS Medical or your dealer to learn more about how to determine sizing. MODEL MODEL NUMBER TYPE...
(3) years from the date Device is delivered to the original purchaser (“Warranty Period”). AIROS Medical warrants the garments for the Devices to be free from defects in workmanship and materials for a period of one (1) year from the date the garments are delivered to the original purchaser.
NOTE: This unit is not field-serviceable. Tampering with or dismantling this unit in any way will void warranty. If you have questions or need assistance, please contact your local authorized dealer. Manufactured for: AIROS Medical, Inc. 2501 Monroe Blvd., Suite 1200 Audubon, PA 19403 1-866-991-6956 www.airosmedical.com...
The AIROS 6 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. Portable and mobile RF communications equipment can affect the AIROS 6 Sequential Compression Device. Technical Description...
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Electromagnetic Emissions The AIROS 6 Sequential Compression Device is intended for use in the electromagnetic environment specified below. The customer or user of the AIROS 6 Sequential Compression Device should assure that it is used in such an environment. EMISSIONS...
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Electromagnetic Immunity The AIROS 6 Sequential Compression Device is intended for use in the electromagnetic environment specified below. The customer or user of the AIROS 6 Sequential Compression Device should assure that it is used in such an environment. Immunity Test...
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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 AIROS 6 Sequential Compression Device is used exceeds the applicable RF compliance level above, the AIROS 6 Sequential Compression Device should be observed to verify normal operation.
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The AIROS 6 Sequential Compression Device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the AIROS 6 Sequential Compression Device can help prevent electromagnetic interference by maintaining a minimum distance between...
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Questions and answers
LOST THE POWER CORD, NEED REPLACEMENT FOR THE ENTIRE AC POWER CIRD
To obtain a replacement AC power cord for the AIROS Medical AIROS 6, contact your local authorized dealer.
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I’m getting an E02 error but the garment does not deflate.