STRUB GMBH
DE-MF-000034376 · Germany · Rohrbach
STRUB GMBH is registered in the European database on medical devices as a manufacturer, with 33 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 33 |
|---|
Among these devices, 6 are declared active.
Devices declared under this manufacturer
- EMS7
- Eureca
- Jondal
- Longchair
- Phönix
- Phönix Lounge
- Smartlift Energy
- Smartlift Syncro
Showing 12 of 33 declared devices.
Catalogue references include EM00-7302-C04-K02, EM00-7302-STD-K01, JO00-6021-STD-K01, LC00-6011-STD-K03, LC00-6013-STD-K05, LC00-6022-STD-K02.
European nomenclature codes declared: V080202, B99, V08020101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 33 |
| 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 | 33 |
|---|---|
| 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. STRUB GMBH was not found in either the U.S. or the Canadian register.