Paul Boettger GmbH & Co. KG
DE-MF-000022524 · Germany · Bodenmais
Paul Boettger GmbH & Co. KG is registered in the European database on medical devices as a manufacturer, with 25 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 7 |
|---|
Catalogue references include 06-013-0100, 06-044-0002, 06-053-0100, 06-065-0004, 06-065-0104, 06-065-1104.
European nomenclature codes declared: W05010203, V0499, W05019001, W050180.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 25 |
| 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 | 25 |
|---|---|
| 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. Paul Boettger GmbH & Co. KG was not found in either the U.S. or the Canadian register.