PharmaFit
DE-MF-000046694 · Germany · Stralendorf
PharmaFit is registered in the European database on medical devices as a manufacturer, with 17 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 17 |
|---|
Devices declared under this manufacturer
- Heilmoorpackung
- Moorpaste Bademoor 1000 ml
- Moorpaste Fußbad 500 ml
- Moorpaste für die Hand Manupack
- Schlickpaste 1000 g
- Streichmoorpaste 1250 g
- Streichmoorpaste 5 kg
- Trockenschlick 1000 g
- Trockenschlick 240 g
- Trockenschlick 50 g
- Wärmeträger Gr.1
- Wärmeträger Gr.2
Showing 12 of 17 declared devices.
Catalogue references include 0012, 0020, 0041, 0042, 0052, 0087.
European nomenclature codes declared: M9001.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 17 |
| 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 | 17 |
|---|---|
| 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. PharmaFit was not found in either the U.S. or the Canadian register.