SCORPION
FR-MF-000000158 · France · Romagnat
SCORPION is registered in the European database on medical devices as a manufacturer, with 25 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 25 |
|---|
Most frequent device types declared: Inserts de détartrage SCORPION.
Devices declared under this manufacturer
- CLEF-EM Scorpion
- CLiPPER Scorpion
- Insert Scorpion AIR
- Insert Scorpion AIRw
- Insert Scorpion BEM
- Insert Scorpion BSI
- Insert Scorpion EPKP
- Insert Scorpion EPLM
- Insert Scorpion I-AIR
- Insert Scorpion I-AIRw
- Insert Scorpion I-KA
- Insert Scorpion I-KP
Showing 12 of 25 declared devices.
Catalogue references include BEM, BSI, CLiPPER, EPKP, I-AIRw, I-KP.
European nomenclature codes declared: Z12119001, Z12119080.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 25 |
| 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 | 25 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | SCORPION |
North American profile: Canada only. SCORPION holds a Canadian licence but was not found in the U.S. register.