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: MULTIFLEX, ASPIFLEX, PROLEX, DEVIALEX, COMPOFLEX.
Among these devices, 508 are declared sterile.
No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 509 |
| Country of registration | Italy |
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
0425-MDR-030144-00 | issued | 2030-09-09 |