Bisico GmbH
DE-MF-000005871 · Germany · Bielefeld
Bisico GmbH is registered in the European database on medical devices as a manufacturer, with 46 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 46 |
|---|
Among these devices, 37 are declared implantable.
Catalogue references include 03710, 75005, 75007, 75200, 75241, 76500.
European nomenclature codes declared: Q01010103, Q01020605, Q010299, Q01010104, Q01010202, Q01010402.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 46 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
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. Bisico GmbH was not found in either the U.S. or the Canadian register.