BACK2SLEEP
Active in EUDAMEDFrancefrom SRN EUDAMED SRN FR-MF-000034642
- Devices
- 13
- Registrations
- EUDAMED
At a glance
Market reach
- European Union
- EUDAMED actor
What BACK2SLEEP makes
The company manufactures nasal airway stents, including sizes labeled S, M, L, and XL, designed to maintain patency in the nasal passages. It also produces a range of snoring relief devices under the Back2Sleep brand, including kits and packs of varying sizes (S, L, XL) intended for at-home use.
All listed devices fall under EU Class I regulation and are registered in the EUDAMED database. The manufacturer is based in France and adheres to EU medical device compliance requirements.
Catalogue
Search and filter all 13 devicesCompany details
- EUDAMED SRN
- FR-MF-000034642
- SRN (system / procedure pack)
- FR-PR-000034641
- EU VAT number
- FR26914906268
- EUDAMED status
- Active
- EUDAMED registered name
- BACK2SLEEP
- Registered address
- 188, Rue de Rivoli, 75001, PARIS, France
- Website
- www.back2sleep.eu
- [email protected]
- Phone
- +140410004
- PRRC contact
- Olivier Fourcade
From the company website
Soft medical-grade silicone nasal stent for snoring and mild sleep apnea. Mask-free, machine-free, made in Germany. CE-marked class I medical device.
Frequently asked questions
How many devices does BACK2SLEEP have in the registry?
The registry currently lists 13 devices for BACK2SLEEP. Devices recorded under merged duplicate company entries are counted once.
Which registries list BACK2SLEEP's devices?
Among its 13 most recently registered devices, BACK2SLEEP has devices listed in EUDAMED (13 devices).
What risk classes do BACK2SLEEP's devices fall under?
Among its 13 most recently registered devices, the classes recorded for BACK2SLEEP's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from BACK2SLEEP in the registry?
The most recently registered devices listed for BACK2SLEEP include Back2Sleep, Back2Sleep Snorekit, Back2Sleep pack S and Stent L.