Wulff Med Tec GmbH
DE-MF-000010006 · Germany · Fedderingen
Wulff Med Tec GmbH is registered in the European database on medical devices as a manufacturer, with 534 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 534 |
|---|
Devices declared under this manufacturer
- AirForm II
Showing 12 of 534 declared devices.
Catalogue references include 4PW3W1100LS, MP.KA8-200.100.18, MP.KO1-180.80.14, MP.KW7-190.90.14, MP.KW7-198.73.16(N-PAL13), MV.CD1-190.90.14-RZ.
European nomenclature codes declared: V080702.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 534 |
| 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 | 534 |
|---|---|
| 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. Wulff Med Tec GmbH was not found in either the U.S. or the Canadian register.