GERWING Medizinprodukte Gerd Riester e.K.
DE-MF-000006156 · Germany · Jungingen
GERWING Medizinprodukte Gerd Riester e.K. is registered in the European database on medical devices as a manufacturer, with 80 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 80 |
|---|
Most frequent device types declared: Beinkatheterhalter, Patientenhalter, Universal-Schlauchhalter.
Devices declared under this manufacturer
- Beinkatheterhalter
- Halteband
- Haltegurt
- OP-FIX DuoCLIP
- OP-FIX mit CLIP
- OP-FIX mit HAKEN
- OP-FIX-Band
- Tracheo-FIX
- Unrinbeinbeutel-Halter
Showing 12 of 80 declared devices.
Catalogue references include GE 01-30x5 FI, GE 01-32x5 G, GE 01-32x5 GM, GE 01-40x5 NFI, GE 01-80x5 NFI, GE 03-1011 G.
European nomenclature codes declared: V80, R01038099, U0180.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 80 |
| 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 | 80 |
|---|---|
| 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. GERWING Medizinprodukte Gerd Riester e.K. was not found in either the U.S. or the Canadian register.