Curtis Health Caps S.A.
PL-MF-000007127 · Poland · Wysogotowo
Curtis Health Caps S.A. is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 1 |
|---|---|
| Class I | 5 |
Devices declared under this manufacturer
- DOZ MED SIMETICON MAX
- Porost islandzki – syrop
- SIMETHICONE
- Simethicon 80 mg
- Simetisan Control
- Symetykon MAX
Catalogue references include BM004, M011a, M011b, M011c, M011d, M012.
European nomenclature codes declared: G0401,V0299, V9017.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 6 |
| Country of registration | Poland |
⚠️ 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. Curtis Health Caps S.A. was not found in either the U.S. or the Canadian register.