bioSight GmbH
DE-MF-000014399 · Germany · Kassel
bioSight GmbH is registered in the European database on medical devices as a manufacturer, with 64 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 62 |
|---|---|
| Class IIb | 2 |
Devices declared under this manufacturer
- BASIC by buchner® Flächendesinfektion
- Careful Instrumentendesinfektion
- Careful Schnelldesinfektion protect
- DESTAsept® SW clean
- DESTAsept® SW sensitive
- DIROMATIC-FLUID forte
- INTERMED Instrumentendesinfektion ECO
- INTERMED Instrumentenreiniger
- INTERMED Schnelldesinfektion N
- INTERMED Wipes SENSITIVE
- SAFELINE® Quick Des N Lemon
- SAFELINE® Quick Des Wipes N
Showing 12 of 64 declared devices.
Catalogue references include 09925-N, 09980, 210052, 211927, 211990, 4893042.
European nomenclature codes declared: D0701, D0901, D0899, D0902, D01010102, D0502.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 64 |
| 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 | 64 |
|---|---|
| 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. bioSight GmbH was not found in either the U.S. or the Canadian register.