Tactile Medical Actitouch, Руководство пользователя

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Customer Service Toll-Free: 866.435.3948
3 .2 Cautions
• Regularly check the status indicator located at the top of the control unit while
using ACTitouch. The green light on the control unit indicates the control unit
is charged and on. A flashing red status light (and periodic audible alarm)
indicates that battery power is low. No light indicates the power is off.
• Ensure that the device is clean and dry prior to storage.
• Do not immerse the ACTitouch System in water, or spill liquid on the control
unit. The device is not waterproof, and exposure to liquid may damage the
control unit or Compression Sleeve. If the device becomes soaked with fluid,
discontinue use of the device.
• Do not allow the Compression Sleeve to come into contact with sharp objects.
• Do not expose the Undersock, Compression Sleeve or control unit to excessive
heat or open flames, such as cigarettes, portable heaters, etc.
Indications and Contraindications
CHAPTER 4
Rx Only
U.S. Federal law restricts this device to sale by, or on the order of, a licensed
healthcare professional.
4 .1 Indications
The ACTitouch System provides graduated compression in both sustained and
intermittent settings for use in:
• Enhancing venous return;
• Reducing venous leg ulcer healing time;
• Treatment and promotion of healing of stasis dermatitis and venous stasis
ulcers;
• Treatment of chronic venous insufficiency;
• Reducing edema due to venous stasis;
• Treatment of lymphedema.