Karl Berg GmbH
DE-MF-000005811 · Germany · Engen
Karl Berg GmbH is registered in the European database on medical devices as a manufacturer, with 13 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 13 |
|---|
Devices declared under this manufacturer
- BISSNEHMEWACHS in Platten (gelb) 3,0 mm 500 gr.
- BISSNEHMEWACHS in Platten (rosa) 3,0 mm 500 gr.
- BISSNEHMEWACHS in Stangen (gelb) 2500 gr.
- BISSNEHMEWACHS in Stangen (gelb) 450 gr.
- BISSNEHMEWACHS in Stangen (rosa) 2500 gr.
- BISSNEHMEWACHS in Stangen (rosa) 450 gr.
- BISSNEHMEWACHS in Stangen (weiß) 2500 gr.
- BISSNEHMEWACHS in Stangen (weiß) 450 gr.
- Orthodontic - Wachssticks neutral (weiß)
- Protektionswachs (weiß) 5,0 mm
- Tribos Modellierwachs,Block,gingiva 100g.
- Tribos Plattenwachs H, hart, gingiva, 1000g
Showing 12 of 13 declared devices.
Catalogue references include 40000, 40001, 40002, 40003, 40006, 40007.
European nomenclature codes declared: Q01020199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 13 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
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. Karl Berg GmbH was not found in either the U.S. or the Canadian register.