Petermann GmbH
DE-MF-000013598 · Germany · Dombühl
Petermann GmbH is registered in the European database on medical devices as a manufacturer, with 153 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 153 |
|---|
Devices declared under this manufacturer
- Alpha Bettleiter
- Alpha Drehscheibe
- Alpha Gleitmatte
- Alpha Hebematte
- Alpha Soft-Drehscheibe
- Antirutschmatte
- Caremaster M
- OnlyU PEM-Einweg-Bezug
- Positionierungskeil
- Rettungstuch XXL
- Rollboard Neo Genius Bezug rot
- Rollboard Vision rot
Showing 12 of 153 declared devices.
Catalogue references include PM-2015, PM-2095, PM-4016, PM-5080, PM-7011, PMF-9051.
European nomenclature codes declared: Y99, V080504, V0899, V0899,Y99, Y093399, Y122499.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | Petermann GmbH (DE) · FDA 9615109 |
| Devices in EUDAMED | 153 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 153 |
|---|---|
| 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: United States only. Petermann GmbH is registered in the United States but was not found in the Canadian register.