MJK INSTRUMENTS
FR-MF-000017000 · France · MARSEILLE
MJK INSTRUMENTS is registered in the European database on medical devices as a manufacturer, with 15 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 15 |
|---|
Most frequent device types declared: Blade holder, Bone block holder, Surgical retractor.
Devices declared under this manufacturer
- MJK INSTRUMENTS
Showing 12 of 15 declared devices.
Catalogue references include AP001, CL021, IH001A, IH001TB, IH002, KE001.
European nomenclature codes declared: L150202, L010103, L150399, V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 15 |
| 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 | 15 |
|---|---|
| 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. MJK INSTRUMENTS was not found in either the U.S. or the Canadian register.