Saljol GmbH
DE-MF-000015913 · Germany · Maisach
Saljol GmbH is registered in the European database on medical devices as a manufacturer, with 44 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 44 |
|---|
Most frequent device types declared: Saljol Allround Rollator, Saljol Carbon Rollator, Saljol Duschhocker, Saljol Wohnraumrollator.
Devices declared under this manufacturer
- Saljol Allround Rollator
- Saljol Carbon Rollator
- Saljol Duschhocker
- Saljol Wohnraumrollator
Showing 12 of 44 declared devices.
Catalogue references include 4058789016510, 4058789016527, 4058789016855, 4058789017180, Saljol Allround Rollator AR54 Pearl Grey, Saljol Carbon Rollator CR54 Matt Black.
European nomenclature codes declared: Y120606, Y120609, Y093303.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 44 |
| 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 | 44 |
|---|---|
| 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. Saljol GmbH was not found in either the U.S. or the Canadian register.