PHYSIOMED ELEKTROMEDIZIN AG
DE-MF-000009637 · Germany · Schnaittach
PHYSIOMED ELEKTROMEDIZIN AG is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 7 |
|---|
Most frequent device types declared: DEEP OSCILLATION, IONOSON, PHYSIODYN, PHYSIOVAC, vocaSTIM®.
Among these devices, 7 are declared active.
Devices declared under this manufacturer
- DEEP OSCILLATION Evident
- DEEP OSCILLATION Personal
- DEEP OSCILLATION Personal Home
- IONOSON-Expert
- PHYSIODYN-Expert
- PHYSIOVAC-Expert
- vocaSTIM®-Master
Catalogue references include 02034-G, 02035-G, 02040-G, 02040-G-LIPÖDEM, 02041-G, 02042-G.
European nomenclature codes declared: Z12062799, Z120601, Z120602.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | PHYSIOMED ELEKTROMEDIZIN AG (DE) · FDA 3002892330 |
| Devices in EUDAMED | 7 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 7 |
|---|---|
| Found in the U.S. device database | 2 |
| Share | 28.6 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | PHYSIOMED ELEKTROMEDIZIN AG |
North American profile: Both markets. PHYSIOMED ELEKTROMEDIZIN AG is registered in both the United States and Canada.