Beromed GmbH Hospital Products
DE-MF-000007458 · Germany · Berlin
Beromed GmbH Hospital Products is registered in the European database on medical devices as a manufacturer, with 203 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 203 |
|---|
Among these devices, 203 are declared sterile.
Devices declared under this manufacturer
- BEROFINE
- BEROFINE SAFETY
Showing 12 of 203 declared devices.
Catalogue references include 911501EB, 911600BB, 911617EB, 911624BB, 911730EB, 911808EB.
European nomenclature codes declared: A0101010101, A0101010102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 203 |
| 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 | 203 |
|---|---|
| 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. Beromed GmbH Hospital Products was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
G10 044082 0047 | issued | 2029-01-09 |