Kunststofftechnik Buelck GmbH
DE-MF-000045894 · Germany · Blomesche Wildnis
Kunststofftechnik Buelck GmbH is registered in the European database on medical devices as a manufacturer, with 12 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 12 |
|---|
Most frequent device types declared: HG04120, HG04121, HG04124, HG04126, HG04127.
Devices declared under this manufacturer
- ARRIGA
- ARRIVA
Catalogue references include 04121, 04124, 04127, 04130, 04131, 04132.
European nomenclature codes declared: Y181806.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 12 |
| 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 | 12 |
|---|---|
| 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. Kunststofftechnik Buelck GmbH was not found in either the U.S. or the Canadian register.