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: Flat Head Screw, IIa_Drill, IIa_Trial Head, IIa_Trial Plug, I_Impact Instrument.
Among these devices, 10 are declared sterile, 10 implantable, 94 reusable.
Devices declared under this manufacturer
- Cylindrical Medullary Cavity Drill Ø 12
- Cylindrical Medullary Cavity Drill Ø 16
- Drill Pin Adaptor Zimmer-Connection
- Modular Weight, 1.4301
- Stem Drill L110
- Trial Head with X-Ray-Pin Ø22M 12/14
- Trial Head with X-Ray-Pin Ø28M 12/14
- Trial Head with X-Ray-Pin Ø32S 12/14
- Trial Head with X-Ray-Pin Ø36L 12/14
- X-Ray Template Bipolar Head Ø28 Uneven Sizes, Scale:1,15:1
- X-Ray Template Expersus Femoral Stem cemented, STD 135° HD32 Scale 1.1
- X-Ray Template NANOS D32, Scale 1,15:1
Showing 12 of 104 declared devices.
Catalogue references include 367-2018, 367-244, 367-245, 502-221, 506-2107, 512-281.
European nomenclature codes declared: V9099, L091199, L091102, P09088007, L0903, L091104.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 104 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 104 |
|---|---|
| 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. OHST Medizintechnik AG was not found in either the U.S. or the Canadian register.