SUBLIMED
FR-MF-000007546 · France · Moirans
SUBLIMED is registered in the European database on medical devices as a manufacturer, with 23 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 23 |
|---|
Among these devices, 14 are declared active.
Devices declared under this manufacturer
- Accessoire ceinture/ soutien gorge VitaliTENS
- Application mobile VitaliTENS pour Android
- Application mobile VitaliTENS pour iOS
- Brassard VitaliTENS Taille Standard
- Brassard VitaliTENS Taille XS
- EndoTENS Android app
- VitaliTENS
- VitaliTENS mini
- actiTENS
- actiTENS armband (XS size)
- actiTENS belt/ bra accessory
- actiTENS iOS app
Showing 12 of 23 declared devices.
Catalogue references include 8703698, 8703700, 8703703, 8704427, END2AA100, SBM1AB001.
European nomenclature codes declared: Z120601.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | SUBLIMED (FR) · FDA 3015588280 |
| Devices in EUDAMED | 23 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 17 |
|---|---|
| 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: United States only. SUBLIMED is registered in the United States but was not found in the Canadian register.