Why is my Tactile Medical Equipment compression sleeve not inflating?
The compression sleeve might not be inflating because the control unit hasn't been securely inserted into the compression sleeve, the control unit needs charging, or the control unit hasn't been switched on. Also, the MUTE button may have been activated while operating in sustained mode.
What to do if my Tactile Medical Equipment control unit does not respond to buttons?
If the control unit doesn't respond to button presses, it might need to be charged or switched on. Try charging the control unit, or switching it on. You may also need to reset the event log by removing the control unit from the Compression Sleeve, then pressing and holding the MUTE button for ten seconds until the LCD flashes. Also, try holding the button down for a longer period of time (e.g., Two [2] seconds).
Why won't my Tactile Medical Equipment control unit operate in sustained compression mode?
The control unit might not operate in sustained compression mode if it hasn't been securely inserted into the Compression Sleeve, needs to be charged, or hasn't been switched on. Another reason could be that the MUTE button has been activated, or the event log needs to be reset. To reset the event log, remove the control unit, press and hold the MUTE button for ten seconds until the LCD flashes.
General| Type | Pneumatic Compression Device |
|---|---|
| Portability | Portable |
| Power Source | Rechargeable Battery |
| Garment Options | Arm, Leg |
| Indication | Lymphedema |
Explains the sustained compression mode of the device and its pressure delivery.
Details the intermittent pneumatic compression mode and its operation.
Lists essential safety precautions and warnings for using the device.
Provides important cautionary advice for device operation and maintenance.
Outlines the medical conditions for which the ACTitouch System is indicated.
Lists medical conditions where the ACTitouch System is contraindicated.
Identifies and explains the functions of the ACTitouch control unit and sleeve.
Guides the user through the initial setup and preparation of the device.
Provides instructions on how to properly charge the ACTitouch device.
Details the steps for applying the ACTitouch System to the leg and foot.
Explains how to turn on the device in Sustained Compression Mode.
Describes how to activate and deactivate the mute function in Sustained Compression Mode.
Explains how to use the Intermittent Pneumatic Compression Mode.
Details the procedure for turning off and safely removing the ACTitouch System.
Instructs on how to properly remove the ACTitouch System from the body.
Provides instructions for cleaning and disinfecting the device components.
Offers guidance on proper storage and handling of the ACTitouch System.
Clarifies that the device is maintenance-free and outlines service.
Guides users on the proper disposal of ACTitouch System components.
Details the warranty terms for the ACTitouch System for home users.
Provides contact information for obtaining replacement parts and service.
Outlines the warranty and service agreements for facility use.
Specifies the policy regarding returns and refunds for ACTitouch products.
Lists the United States patents protecting the ACTitouch System.
States the company's policy on product modification and improvement.
Explains the meaning of various symbols used on the ACTitouch device and its packaging.
Describes how to read and interpret the device label on the control unit.
Details the device's compliance with electromagnetic interference standards.
Provides guidance on maintaining safe distances from RF equipment to prevent interference.
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