Summary of Contents for Precision Medical venaone 08-0030
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Lightweight or Cords Model No. 08-0030 Precision Medical Products Customer Support: (800) 604-2487 • info@pmpmed.com • www.pmpmed.com 2217 Plaza Drive, Rocklin, CA 95765 Caution: Federal Law restricts this device to sale by or on the order of a licensed practitioner...
VENAONE OVERVIEW Pneumatic compression is a clinically proven modality for reducing the risks associated with deep vein thrombosis (DVT). VenaOne is a tubeless, portable, lightweight and battery-operated DVT compression system designed specifically for the acute-care setting. VenaOne aids in the prevention of DVT by helping to stimulate blood flow in the legs.
Features and Benefits Portable Lightweight VenaOne’s simple design is fully ambulatory. Weighs less than one pound. Easy One-Touch Operation Battery Operated Controls all functions with just the power button. ~24 hour battery life allows for ease of use and patient compliance. Infection Control Compression The device is designed to help reduce bacterial...
System Contents LED Display Power Button Charging Port VenaOne Wraps (Sold Separately) Part #07-0020 Charging Station (Sold Separately) Part #07-0013 Warning: Only Use Wrap(s) provided by Precision Medical Products...
Battery Indicators & Charging Battery icon: Remains illuminated at all times during operation. All 3 Bars Solid Green: The battery is 100% charged. 2 Bars Solid Green, 1 Bar Flashing: The battery is between 31% and 60% charged. The third bar flashes until fully charged. One Bar Solid Green, 2 Bars Flashing: The battery has 30% charge remaining.
Application Instructions PLACE THE DEVICE IN THE WRAP SEALING THE WRAP(S) The VenaOne Device and Bladder will slide to Once the device is placed inside the wrap, peel the bottom of the Wrap (sold separately). off the backing on the adhesive strip. Then simply fold over and press to seal the wrap.
Pump Alarm Indicators If the device is turned on after an alarm event, the LED will display the previous alarm. High Pressure “HP” In the unlikely event that the device applies higher pressures than normal, a high pressure (HP) alarm will display. If this occurs, power off and restart the system. If the alarm persists, remove the device from service and replace.
Device Handling DEVICE DISPOSAL All contaminated products or accessories should be disposed of appropriately according to hospital policy and state law, taking environmental factors into consideration. When use is completed, or the patient is discharged, remove the device, and discard only the wrap(s). DO NOT DISPOSE OF THE DEVICE DISPOSE OF THE WRAP ONLY DO NOT USE SCISSORS...
Do not handle the leg cuffs with any sharp objects. If a bladder is punctured or you notice a leak, do not attempt to repair the device or cuffs. Replacement devices will be made available to you by your local sales representative. Avoid folding or creasing the bladder during the use and transportation of the devices.
EMC GUIDANCE Warning: Warning: operating normally. Warning: result in improper operation. Warning: TECHNICAL DESCRIPTION disturbances for the excepted service life. GUIDANCE AND MANUFACTURER’S DECLARATION - ELECTROMAGNETIC EMISSIONS VenaOne is intended for use in the electromagnetic environment specified below. The customer or the user of VenaOne should assure that it is used in such an environment.
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GUIDANCE AND MANUFACTURER’S DECLARATION - ELECTROMAGNETIC IMMUNITY VenaOne is intended for use in the electromagnetic environment specified below. The customer or the user of VenaOne should assure that it is used in such an environment. Immunity Test IEC 60601 COMPLIANCE ELECTROMAGNETIC ENVIRONMENT GUIDANCE TEST LEVEL LEVEL...
WARNINGS • The VenaOne wraps are designed for single patient use only. in accordance with instructions, may cause harmful • The device is to be used only by the patient there is no guarantee that interference will not occur prescribed, and only for its intended use. •...
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