HAIDER BIOSWING GmbH
DE-MF-000008765 · Germany · Pullenreuth
HAIDER BIOSWING GmbH is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 5 |
|---|
Most frequent device types declared: 1, 100, 2, 202, compact.
Devices declared under this manufacturer
- BIOSWING Posturomed 202
- BIOSWING Posturomed compact
- BIOSWING Propriomed 1
- BIOSWING Propriomed 100
- BIOSWING Propriomed 2
Catalogue references include Posturomed 202, Posturomed compact, Propriomed 1, Propriomed 100, Propriomed 2.
European nomenclature codes declared: Z120603.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 5 |
| 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 | 5 |
|---|---|
| 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. HAIDER BIOSWING GmbH was not found in either the U.S. or the Canadian register.