CRISPIN MEDICAL
FR-MF-000048871 · France · La Seguiniere
CRISPIN MEDICAL is registered in the European database on medical devices as a manufacturer, with 16 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 16 |
|---|
Most frequent device types declared: Light-curing resin syringe, Liquid resin, Metal utensil, Silicone paste jar, Silicone syringe.
Devices declared under this manufacturer
- Applicateur A
- Applicateur B
- Bonding primer 5ml
- Fil titane Ø0,14x20cm
- Fil titane Ø0,16x20cm
- PODOCOMP D
- PODOCOMP F
- PODOCOMP L
- PROTECSIL SILIPOD 5 - 2x50g
- Protecsil SILIPOD 5 - 2x250g
- SILIPOD 20 - 2x250g
- SILIPOD 20 - 2x50g
Showing 12 of 16 declared devices.
Catalogue references include PEORA1049, PEORA1051, PEORA1057, PEORI1019, PEORI1020, PEORI1022.
European nomenclature codes declared: Q01020102, Q01010104, Q010405, L159013.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 16 |
| 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 | 16 |
|---|---|
| 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. CRISPIN MEDICAL was not found in either the U.S. or the Canadian register.