Poirot Plastique Industrie Médical
FR-MF-000023833 · France · senones
Poirot Plastique Industrie Médical is registered in the European database on medical devices as a manufacturer, with 12 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 12 |
|---|
Devices declared under this manufacturer
- 1-FIX
- 1-Guard : ouvre bouche
- 1-Guard Mini
- 1-Guard plus Eco
- 1-Guard plus mini: ouvre bouche de petite taille avec bandeau
- 1-Guard plus: ouvre bouche avec bandeau
- 1-Trap
- 1-guard plus mini
- Guard RMS
- Polytrap
Catalogue references include 10017130, 10017130/R, 10018000, 10018000/R, 100180005, 10018002.
European nomenclature codes declared: G0380, G0305010201.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 12 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 12 |
|---|---|
| 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. Poirot Plastique Industrie Médical was not found in either the U.S. or the Canadian register.