Stiplastics
FR-MF-000000826 · France · SAINT MARCELLIN
Stiplastics is registered in the European database on medical devices as a manufacturer, with 274 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 274 |
|---|
Most frequent device types declared: 32121D, Canule, Coton, KIT RECHARGE, Pansement.
Among these devices, 211 are declared with a measuring function.
Devices declared under this manufacturer
- HEMOBOX
- Hemobox
- NAAPREP
- SEROPHY
- VIATRIS
Showing 12 of 274 declared devices.
Catalogue references include 3110432 IND01, 3110632 HYG001, 3130633, 3142520, 3142633, 3270221 100100.
European nomenclature codes declared: V0399, A99, R03010302, V9099, V901603, R05010399.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | STIPLASTICS (FR) · FDA 3009494725 |
| Devices in EUDAMED | 274 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 274 |
|---|---|
| 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: United States only. Stiplastics is registered in the United States but was not found in the Canadian register.