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Information for patients - 2

Information on the usage of the FlowOx™ system. FlowOx™ is used for the treatment of Peripheral Arterial Disease (PAD), e.g. Intermittent Claudication and Critical Limb Ischemia, as well as, diabetic and pressure wounds. FlowOx™ is a medical device that operates using cyclical negative pressure (-40 mmHg). What is PAD, Intermittent Claudication and Critical Limb Ischaemia? You can develop a condition called PAD when the arteries in your legs become blocked and your legs don’t receive enough blood or oxygen. An early stage of PAD is called Intermittent Claudication (IC). IC is characterized...

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Information for patients - 3

How does the FlowOx™ system work? FlowOx™ generates pulsating negative pressure inside the boot which draws blood down into the leg, improving skin blood flow and oxygenation. This is due to a combination of dilatation of the arterioles and increased arteriovenous pressure gradient. What are the benefits of using FlowOx™? • Non-invasive, safe and easy to use Can be used in addition to surgical intervention or where surgery is contraindicated May be used on limbs with existing wounds if they are bandaged When should FlowOx™ not be used? • In case of skin infections in the area of application...

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Information for patients - 4

How do I clean the FlowOx™ device? The control unit can be dusted with a damp cloth. Don't use any corrosive cleaners, just water. The pressure chamber can be wiped with antibacterial cleaning wipes. Allow the pressure chamber to dry thoroughly before use. . Troubleshooting What do I do if the pressure chamber becomes misted or clouded? You have been provided sachets (small bags) to help with moisture control. If your pressure chamber becomes misted or clouded, simply place sachets inside the pressure chamber during use.

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Information for patients - 5

Troubleshooting - Continuation What does an E2 error message mean? An E2 message is for a major air leakage. Here's what to do: 1. Turn off the device and remove the foot. 2. Reposition the foot back into the device. Ensure the padding is intact and in the correct position. 3. Place seal around leg, checking the seal for integrity. If there's visible damage, replace with a new seal. 4. Check blue strap around the seal is firmly in place. 5. Turn device on and it will run through a self-test mode. The E2 error isn't going away... 1. Remove the foot. Check integrity of padding and seal. 2....

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Information for patients - 6

Who should I contact if I have any concerns? If during the treatment your medical condition worsens, contact your clinical specialist or responsible wound therapist. For technical issues, contact your local customer service team. Otivio GmbH, Fürstenrieder Straße 279a, 81377 München, Germany E-Mail: hallo@otivio.com Tel: +49 151 28 27 35 36 www.flowox.com

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