Glomin GmbH
DE-MF-000047692 · Germany · Hamburg
Glomin GmbH is registered in the European database on medical devices as a manufacturer, with 37 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 37 |
|---|
Most frequent device types declared: Needleholder.
Among these devices, 37 are declared reusable.
Devices declared under this manufacturer
- GLOMIN
- Glomin
Showing 12 of 37 declared devices.
Catalogue references include G30-50410.33, Laparoscopy, Laparscopy.
European nomenclature codes declared: L1205, L1204.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 37 |
| 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 | 37 |
|---|---|
| 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. Glomin GmbH was not found in either the U.S. or the Canadian register.