Joimax GmbH
DE-MF-000009201 · Germany · Karlsruhe
Joimax GmbH is registered in the European database on medical devices as a manufacturer, with 1 137 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 950 |
|---|---|
| Class IIb | 187 |
Among these devices, 324 are declared sterile, 167 implantable, 571 reusable, 55 active.
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 | Registered with FDA |
|---|---|
| Matched entry | JOIMAX GMBH (DE) · FDA 3005083075 |
| Devices in EUDAMED | 1 137 |
| Country of registration | Germany |
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
G11 049319 0011 | issued | 2029-02-04 |
G10 049319 0007 | supplemented | 2029-01-31 |