Medprin Biotech GmbH
DE-MF-000012291 · Germany · Frankfurt am Main
Medprin Biotech GmbH is registered in the European database on medical devices as a manufacturer, with 155 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class I | 155 |
|---|
Most frequent device types declared: HF-A-668s, HF-A-828, HF-A-988, HF-A-9910, HF-A-996s.
Among these devices, 155 are declared sterile, 155 implantable.
Devices declared under this manufacturer
- NeoDura
- ReDura
- StypCel
Showing 12 of 155 declared devices.
Catalogue references include HF-A-668s, HF-A-988, HF-A-9910, HF-B-428s, HF-C-218s, RDP-105.
European nomenclature codes declared: M040501, P900399.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 155 |
| 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 | 155 |
|---|---|
| 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. Medprin Biotech GmbH was not found in either the U.S. or the Canadian register.