RelaxSensation
DE-MF-000040659 · Germany · Obing
RelaxSensation is registered in the European database on medical devices as a manufacturer, with 18 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 18 |
|---|
Most frequent device types declared: PRO Family.
Among these devices, 18 are declared active.
Devices declared under this manufacturer
- ARORA Lift
- RelaxSensation ARORA Base
- RelaxSensation BASIC
- RelaxSensation ESTHETIC
- RelaxSensation PRO
- RelaxSensation PRO Baby
- RelaxSensation PRO Osteo
- RelaxSensation PRO-S
- RelaxSensation PRO-S Baby
- RelaxSensation PRO-S Beauty
- RelaxSensation PRO-S Osteo
- RelaxSensation RECOVERY
Showing 12 of 18 declared devices.
Catalogue references include ARORA Lift, PRO, PRO Osteo, PRO-S, PRO-S Baby, PRO-S Osteo.
European nomenclature codes declared: V080603.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 18 |
| 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 | 18 |
|---|---|
| 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. RelaxSensation was not found in either the U.S. or the Canadian register.