LABORATOIRES ARION
FR-MF-000025697 · France · MOUGINS
LABORATOIRES ARION is registered in the European database on medical devices as a manufacturer, with 20 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class I | 20 |
|---|
Most frequent device types declared: GS-A2X240-MT, GS-A2X295-MT, GS-A2X540-MT, GS-A2XH-445-MT, GS-A2XH220-MT.
Among these devices, 20 are declared sterile, 20 implantable.
Devices declared under this manufacturer
- Monobloc(r) - Silicone SoftOne(r)
- Monobloc(r) Silicone SoftOne(r)
- Monobloc® – Silicone SoftOne®
Showing 12 of 20 declared devices.
Catalogue references include GS-A2X-540-MT, GS-A2X240-MT, GS-A2X295-MT, GS-A2X320-MT, GS-A2X395-MT, GS-A2X455-MT.
European nomenclature codes declared: P0601020202.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | LABORATOIRES URGO (FR) · FDA 9615662 |
| Devices in EUDAMED | 20 |
| Country of registration | France |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 20 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Similar name found — unverified |
|---|---|
| Matched entry | LABORATOIRES URGO |
⚠️ A similar name exists; unverified — why.
What it holds in Canada
| Licences on record | 11 |
|---|---|
| Currently active | 0 |
| Class 2 devices | 11 |
| First licensed | 2008-05-07 |
Licence types: Device Family (8), Single Device (3).
Licensed under: URGOCELL AG/SILVER, URGOTUL AG/SILVER, URGOTUL ABSORB, URGOTUL, URGOTUL ABSORB BORDER, URGOTUL AG/SILVER.