SYNEK MED
RO-MF-000048751 · Romania · Bucuresti
SYNEK MED is registered in the European database on medical devices as a manufacturer, with 14 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 14 |
|---|
Devices declared under this manufacturer
- Arcum
- CARREFOUR
- SYNEK
- Synek
Showing 12 of 14 declared devices.
Catalogue references include AH-DM21-60x90- 5 pcs, AH-DM22-60X90-10pcs-CR, AH-DM40-60X60, AH-DM41-60X90, PIJ042026, PIJ042026-M.
European nomenclature codes declared: T04010299, T0306.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 14 |
| Country of registration | Romania |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 14 |
|---|---|
| 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. SYNEK MED was not found in either the U.S. or the Canadian register.