Skinexians
Active in EUDAMEDFrancefrom SRN EUDAMED SRN FR-MF-000012209
- Devices
- 1
- Registrations
- EUDAMED
At a glance
Market reach
- European Union
- EUDAMED actor
What Skinexians makes
Skinxians manufactures vacuum suction devices designed for skin and body contouring procedures. These systems are intended for non-invasive treatments to reshape and tighten skin through controlled suction technology.
The company’s portfolio is classified under Class I medical devices and is listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in France.
Catalogue
- Regimes: CE MDD Registry: EUDAMEDGUDID
Company details
- EUDAMED SRN
- FR-MF-000012209
- DUNS number
- 276134694
- EU VAT number
- FR13 479 554 776
- EUDAMED status
- Active
- EUDAMED registered name
- SKINEXIANS
- Registered address
- 360, Avenue Georges et Louis Frèrejean, 38780, Pont-Evêque, France
- Website
- www.skinexians.com
- [email protected]
- Phone
- +33 4 27 69 80 65
- PRRC contact
- Jean Pierre CUBIZOLLES
Frequently asked questions
How many devices does SKINEXIANS have in the registry?
The registry currently lists 1 device for SKINEXIANS. Devices recorded under merged duplicate company entries are counted once.
Which registries list SKINEXIANS's devices?
Among its 1 most recently registered device, SKINEXIANS has devices listed in EUDAMED (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do SKINEXIANS's devices fall under?
Among its 1 most recently registered device, the classes recorded for SKINEXIANS's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from SKINEXIANS in the registry?
The most recently registered devices listed for SKINEXIANS include SKINEXIANS FULLSKIN V7.