Meika Group S.r.l.
IT-MF-000029106 · Italy · Mirandola
Meika Group S.r.l. is registered in the European database on medical devices as a manufacturer, with 509 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 509 |
|---|
Most frequent device types declared: ASPIFLEX, BAGFLEX, COMPOFLEX, CROSSFLEX, DEFLEX.
Among these devices, 508 are declared sterile.
Devices declared under this manufacturer
- AD Plus
- ARTROFLEX
- IN JOINT CELLS
- LAYPOCEX Plus
- LAYPOCEX Plus A CIRCUITO CHIUSO
- LIPOEVOLUTION
- LIPOTISSUE
- MYSTEM
- SKIN
Showing 12 of 509 declared devices.
Catalogue references include ASP1107, ASP2197, ASP3046, MUL2032, MUL8040, R143041050.0.
European nomenclature codes declared: A03020101, A06010103, A0704, A03020199, A03010199, A060204.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 509 |
| Country of registration | Italy |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 509 |
|---|---|
| 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. Meika Group S.r.l. was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
0425-MDR-030144-00 | issued | 2030-09-09 |