WUNDmed GmbH & Co. KG
DE-MF-000010322 · Germany · Abenberg
WUNDmed GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 106 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 106 |
|---|
Most frequent device types declared: 04-037.
Devices declared under this manufacturer
- Akupunkturpflaster
- Ellbogenschutz M
- Ellbogenschutz XL
- Europflaster
- Fußgelenkschutz S
- Handstütze M
- Heftpflaster
- Kinderpflaster Lustige Tiere
- Kinesiologie-Tape schwarz
- Mullbinde
- Sport Tape
- Sportfixierband
Showing 12 of 106 declared devices.
Catalogue references include 02-041, 02-069, 02-128, 03-008, 04-002-M, 04-006-M.
European nomenclature codes declared: M0599, M03040299, M030402030102, M0303010201, M9001, V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 106 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 106 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. WUNDmed GmbH & Co. KG was not found in either the U.S. or the Canadian register.