PIP Global Safety France
FR-MF-000023170 · France · Villepinte
PIP Global Safety France is registered in the European database on medical devices as a manufacturer, with 30 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 30 |
|---|
Devices declared under this manufacturer
- DexPure 800-81 10-XL
- DexPure 800-81 7-S
- DexPure 800-81 9-L
- DexPure 800-91
- DexPure 800-91 10-XL
- DexPure 800-91 8-M
- DexPure 800-91 9-L
- DexPure 801-21
- DexPure 801-30 10-XL
- DexPure 801-30 9-L
- DexPure 801-95
- DexPure 803-81
Showing 12 of 30 declared devices.
Catalogue references include 1007046, 45 800-81 7-S, 45 801-21 10XL, 45 801-21 7-S, 45 801-21 8-M, 45 801-30 9-L.
European nomenclature codes declared: T01020204, T010201, V08050101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 30 |
| 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 | 30 |
|---|---|
| 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. PIP Global Safety France was not found in either the U.S. or the Canadian register.