Febromed GmbH & Co. KG
DE-MF-000009287 · Germany · Oelde
Febromed GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 32 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 32 |
|---|
Most frequent device types declared: Gebärwannen.
Devices declared under this manufacturer
- Dullstein - Gebärhocker ALU
- Gebärsystem - Multitrac
- Gebärsystem - Pelvitrac
- Oceanis
- Schwenkbares Halteseil - Variotrac Standversion
- Schwenkbares Haltesystem - Deckenversion get up 1700
- Schwenkbares Haltesystem - Deckenversion get up MRT 1700
- Schwenkbares Haltesystem - Deckenversion get up MRT 2600
- Schwenkbares Haltesystem - Multilift get up
- Schwenkbares Haltesystem - Standversion get up 2600
- Schwenkbares Haltesystem - Wandversion get up 2600
- Schwenkbares Haltesystem - get up Teleskop
Showing 12 of 32 declared devices.
Catalogue references include PTRAC-2000, VARIOS-7000, get up - Multilift, get up - Tele, get up 1700D, get up 1700D MRT.
European nomenclature codes declared: V08050399, V080299,V0899, Z12080305,Z12080399, V0899, V080299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 32 |
| 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 | 32 |
|---|---|
| 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. Febromed GmbH & Co. KG was not found in either the U.S. or the Canadian register.