Walter Haverich GmbH
DE-MF-000013187 · Germany · Bielefeld
Walter Haverich 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 |
|---|
Catalogue references include DR 16/16 TE, DR 24/20 TE, DR 24/20 TE klappbar, DR 24\, DR 26/20 ALU TE, TH 20\.
European nomenclature codes declared: Y121899, Y121806.
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.
Device-level evidence
| Devices with a numeric GTIN | 46 |
|---|---|
| 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. Walter Haverich GmbH was not found in either the U.S. or the Canadian register.