OHST Medizintechnik AG
DE-MF-000008887 · Germany · Rathenow
OHST Medizintechnik AG is registered in the European database on medical devices as a manufacturer, with 104 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 94 |
|---|---|
| Class IIb | 10 |
Most frequent device types declared: I_X-Ray Template, IIa_Trial Head, Flat Head Screw, IIa_Drill, IIa_Trial Plug.
Among these devices, 10 are declared sterile, 10 implantable, 94 reusable.
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 | 104 |
| Country of registration | Germany |
⚠️ 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.