Full reimbursement if eligible. FOOTMENDER IS A CLASS IIA MEDICAL DEVICE
Footmender is approved as a class IIa medical device (in accordance with the European Medical Device Legislation) for treating dry feet, calluses, corns and cracked heels. The medical device classification means that the effect is well documented/proven and that it is manufactured under carefully controlled conditions in accordance with comprehensive regulations. Thanks to the classification as a class IIa medical device, Footmender may be used on damaged skin. We are certified according to ISO 13485 and apply the principles of ISO 14971 for risk management.
Footmender is a unique product with unique properties. That is why a European patent has been obtained (EP2522342) from the EPC (European Patent Convention), which grants patents in 40 European countries. In addition, an international patent has also been obtained, PCT (Patent Cooperation Treaty), which enables patent protection in a further 106 countries around the world such as the USA, Japan and Australia.
Now available on prescription
Footmender All in One Diabetic is now available on prescription. Ask your GP, Diabetes specialist or your Podiatrist for more information. Full reimbursement if eligible. PIP CODE: 802-2238.
In a published study, where design and implementation were pre-approved by the Medical Products Agency in Sweden, Footmender has demonstrated very good results in treating dry skin, calluses and cracked heels.