Indications for Use: The VenaPro Vascular Therapy System is intended to be an easy to use portable system, prescribed by a physician, for use in the home or clinical setting to help prevent the onset of DVT in patients by stimulating blood flow in the extremities (simulating muscle contractions). ...
The use of accessories, power supplies and cables other than those specified, with the pal waste and must be collected separately. Contact an authorized representative of the exception of components sold by the manufacturer of the VenaPro as replacement manufacturer for information concerning the decommissioning of your equipment.
Each package contains: • One right compression cuff • One left compression cuff • One AC adapter and battery charger • One VenaPro operator’ s manual The cuff is made of: • Polyester 80% • PU Foam 10% • PVC 10%...
INSTRUCTIONS SYSTEM OVERVIEW If necessary, contact your local Customer Service representative for assistance setting up, using or maintaining the device, or to report unexpected operation or events. POWER OFF: Unit is in “sleep” mode. No visible LED illumination. POWER ON: Unit powers up with GREEN LED illuminated (flashing GREEN if connected to charger and battery is charging, or YELLOW can be illuminated if battery is LOW).
APPLICATION Left Leg Pictured TURNING THE DEVICE ON When both wraps are secured on your legs, they should look When the wraps are secured on your CALF CUFF APPLICATION like the picture above. legs PRESS and HOLD the WHITE power Wrap the cuff around the calf and secure the Velcro to hold it in place.
CLEANING AND DISINFECTING NOTE: Inspect the VenaPro unit and follow the cleaning and disinfecting procedures prior to each use. WARNING: Device must be turned off and disconnected from the wall outlet prior to and during cleaning or disinfecting and for storage between uses. See Storage section for instructions on proper storage.
EMISSIONS CLASS B GUIDANCE AND MANUFACTURER’S DECLARATION - ELECTROMAGNETIC EMISSIONS The VenaPro is intended for use in the electromagnetic environment specified below. The customer or the user of the VenaPro should assure that it is used in such an environment.
GUIDANCE AND MANUFACTURER’S DECLARATION - ELECTROMAGNETIC IMMUNITY The VenaPro is intended for use in the electromagnetic environment specified below. The customer or the user of the VenaPro should assure that it is used in such an environment. Immunity IEC 60601 Test...
TV broadcast cannot be predicted theoretically with accuracy. 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 VenaPro is used exceeds the applicable RF compliance level above, the VenaPro should be observed to verify normal operation.
Takes approximately 4 hours (from depleted state). WARRANTY DJO, LLC will replace VenaPro units for material or workmanship defects for up to 60 days or 500 hours. Copyright 2014 InnovaMedHealth, LLC. All rights reserved. VenaPro is a trademark of Innovamed Health. Patents pending.
GERMANY, AUSTRIA & SWITZERLAND BENELUX DJO Germany GmbH UNITED STATES DJO Benelux Merzhauser Str. 112 Welvaartstraat 8 D-79100 Freiburg DJO Global Inc. 2200 Herrentals Germany 1430 Decision Street Belgium Tel: +49 761 4566 251 Vista Tel: +32 (0) 14 24 80 90...
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Raising the Standard of DVT Prevention MDSS GmbH DJO,LLC Schiffgraben 41 1430 Decision Street 30175 Hannover, Germany Vista, CA 92081-8533, USA DJOglobal .com 30M100_A...
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