GVB-geliMED GmbH
DE-MF-000005314 · Germany · Bad Segeberg
GVB-geliMED GmbH is registered in the European database on medical devices as a manufacturer, with 373 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 373 |
|---|
Devices declared under this manufacturer
- Brustgurt
- EEG Haube GVB Silikon
- EEG Haube Schröter
- Elektroden Board Adapter
- Elektroden Flat
- Elektrodenzopf Base
- Elektrodenzopf Flat
- Elektrodenzopf Pro Flat
- Kinnband
- MultiCap
- MultiCap-Base
- MultiCap-Flat
Showing 12 of 373 declared devices.
Catalogue references include M-23-L, M-T-I1-1525-15, M-T-M-2125-15, M-T-S-2637-15075-A, MZ-NT-M-2025-15, S-Haube-18R.
European nomenclature codes declared: N01010203, Z12100380.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 373 |
| 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 | 373 |
|---|---|
| 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. GVB-geliMED GmbH was not found in either the U.S. or the Canadian register.