Roland Consult Stasche & Finger GmbH
DE-MF-000021413 · Germany · Brandenburg
Roland Consult Stasche & Finger GmbH is registered in the European database on medical devices as a manufacturer, with 10 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 10 |
|---|
Most frequent device types declared: alpha, alpha plus, basic, beta, beta plus.
Among these devices, 9 are declared active.
Devices declared under this manufacturer
- RETI-port/scan 21
Catalogue references include 04-99-3.2-JJ0XXX, 04-99-3.2-JJ1XXX, 04-99-3.2-JJ2XXX, 04-99-3.2-JJ3XXX, 04-99-3.2-JJ4XXX, 04-99-3.2-JJ7XXX.
European nomenclature codes declared: V030203.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 10 |
| 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 | 10 |
|---|---|
| Found in the U.S. device database | 10 |
| Share | 100.0 % |
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. Roland Consult Stasche & Finger GmbH was not found in either the U.S. or the Canadian register.