Woodway GmbH
DE-MF-000009531 · Germany · Weil am Rhein
Woodway GmbH is registered in the European database on medical devices as a manufacturer, with 10 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 10 |
|---|
Devices declared under this manufacturer
- ST 4Front MED
- ST PPS 43 Med
- ST PPS 43 Ortho
- ST PPS 43 Plus
- ST PPS 55 Med
- ST PPS 55 Ortho
- ST PPS 55 Plus
- ST PPS 70 Med
- ST PPS 70 Ortho
- ST PPS 70 Plus
Catalogue references include 161600001, 161600003, 161600005, 161600007, 161600009, 161600011.
European nomenclature codes declared: Z129099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 10 |
| 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 | 10 |
|---|---|
| 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. Woodway GmbH was not found in either the U.S. or the Canadian register.