BUSCH & CO. GmbH & Co. KG
DE-MF-000005963 · Germany · Engelskirchen
BUSCH & CO. GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 8 |
|---|
Devices declared under this manufacturer
- 5772 + D STERI-SAFE PR
- 5772 + HPL STERI-SAFE PR
- 5773 FC03SHOP
- 5773-01 STERI-SAFE wave
- 5773-02 STERI-SAFE wave
- 5773-03 STERI-SAFE wave
- 5773-04 STERI-SAFE wave
- 5773-05 STERI-SAFE wave
Catalogue references include 050581, 050583, 050790, 050792, 050794, 050796.
European nomenclature codes declared: V0799.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | BUSCH & CO. GmbH & Co. KG (DE) · FDA 9611611 |
| Devices in EUDAMED | 8 |
| Country of registration | Germany |
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: United States only. BUSCH & CO. GmbH & Co. KG is registered in the United States but was not found in the Canadian register.