Cyden Limited
UK-MF-000039581 · United Kingdom · Swansea,
Cyden Limited is registered in the European database on medical devices as a manufacturer, with 5 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 5 |
|---|
Among these devices, 5 are declared active.
Authorised representative in the Union: Emergo Europe B.V..
Devices declared under this manufacturer
- SmoothSkin Pure Adapt
- SmoothSkin Pure Ice
- SmoothSkin Pure Mini Lite
Catalogue references include SSB2, SSC1, SSG3.
European nomenclature codes declared: V9099.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | CYDEN Ltd (GB) · FDA 3017400436 |
| Devices in EUDAMED | 5 |
| Country of registration | United Kingdom |
Device-level evidence
| Devices with a numeric GTIN | 5 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | CYDEN LTD |
What it holds in Canada
| Licences on record | 4 |
|---|---|
| Currently active | 0 |
| Class 3 devices | 4 |
| First licensed | 2019-09-30 |
Licence types: Single Device (4).
Licensed under: BRAUN SILK.EXPERT PRO 5, BRAUN SILK.EXPERT PRO 3, BRAUN SILK.EXPERT MINI, BRAUN SKIN I.EXPERT.
North American profile: Both markets. Cyden Limited is registered in both the United States and Canada.