C.HAFNER GmbH + Co. KG
DE-MF-000006304 · Germany · Wimsheim
C.HAFNER GmbH + Co. KG is registered in the European database on medical devices as a manufacturer, with 110 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 110 |
|---|
Among these devices, 110 are declared implantable.
Devices declared under this manufacturer
- AGC NEM Aktivator
- AURUMED Eco 26
- AURUMED KF 55
- AURUMED Pal KF
- Biorplid Keramik, Guss
- CeHa LIGHT CLASSIC, Guss
- Cehadentor 2, Guss
- Orplid C, Guss
- Orplid Inlay, Schweißdraht 0,35 mm
- Orplid Keramik PF, Schweißdraht 0,35 mm
- Orplid LFC, Schweißdraht 0,35 mm
- Orplid PCF, Guss
Showing 12 of 110 declared devices.
Catalogue references include 1016, 1227, 1409, 1502, 1532, 45077.
European nomenclature codes declared: Q010601, A010601.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 110 |
| 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 | 110 |
|---|---|
| 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. C.HAFNER GmbH + Co. KG was not found in either the U.S. or the Canadian register.