Livit Orthopedie B.V.
NL-MF-000000548 · Netherlands · Dordrecht
Livit Orthopedie B.V. is registered in the European database on medical devices as a manufacturer, with 65 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 65 |
|---|
Most frequent device types declared: Kunststof EVO, Metalen EVO, OBP Koker, ORTEAM EVO, OSB + STZ.
Devices declared under this manufacturer
- Kunststof EVO Type 0 Dynafo
- Metalen EVO Type Peroneusveer
- ORTEAM EVO Type Tatum
- Onderbeen Prothesekoker
- Redressiehelm
- Siliconen Duimspalk Kort
- Siliconen Handrol
- Siliconen Pols-Hand Orthese Zonder Duim
- Steunzool 3D geprint
- Zilver Buddyspalk 4 Vingers Orthese
- Zilver Duimorthese Susanne
- Zilver Knucklebender Orthese
Showing 12 of 65 declared devices.
Catalogue references include OA-PH-SIL-DUIMSPALKKORT, OA-PH-SIL-HANDROL, OA-PH-SILVER-2000, OA-PH-SILVER-3000, OA-PH-SILVER-3006, OA-PH-SILVER3011.
European nomenclature codes declared: Y060603, Y06120601, Y06120602, Y060612, Y060606, Y060613.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 65 |
| Country of registration | Netherlands |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 65 |
|---|---|
| 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. Livit Orthopedie B.V. was not found in either the U.S. or the Canadian register.