Peter Brehm GmbH
DE-MF-000006458 · Germany · Weisendorf
Peter Brehm GmbH is registered in the European database on medical devices as a manufacturer, with 3 840 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 2 805 |
|---|---|
| Class I | 541 |
| Class IIb | 494 |
Among these devices, 1 068 are declared sterile, 1 035 implantable, 2 772 reusable.
Devices declared under this manufacturer
- Adapter lang
- Curette abgewinkelt 8/230mm 35° links doppelschneidig
- Einlegematte 470x70
- Einschlägergriff Tibiakonus
- Führungshülse Repomadenschraubendreher
- Klemmschraube M6/+4mm
- MX-Pedikelschraube kanuliert mit CoNi Madenschraube, steril
- PLIF II
- PROBE Spacer
- Primär-Hüftschaft zementfrei
- Setzteller Titanpfanne Keramik
- VEKTOR-Titan Einlegeboden unbestückt Vierkantanschluss
Showing 12 of 3 840 declared devices.
Catalogue references include 42301-35, 42703-01-21, 42727-04-00, 43100-140-02, 60900-100, 61407-08.
European nomenclature codes declared: L091199, P09070304, L091102, L091104, P0909800601,P0909800602, P09088007.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 3 840 |
| 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 | 3 840 |
|---|---|
| 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. Peter Brehm GmbH was not found in either the U.S. or the Canadian register.