CEREDAS
FR-MF-000001858 · France · ANTONY
CEREDAS is registered in the European database on medical devices as a manufacturer, with 57 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 57 |
|---|
Most frequent device types declared: CBC0836, CBC1036, CBC1055, CBC1227, CBCF0836.
Devices declared under this manufacturer
- CYGRIPONE : CANULE TRACHEALE - CALIBREUR DE TRACHEOSTOME
- CYTUBEMAJOR
- CYTUBEMAJOR : CANULE TRACHEALE - CALIBREUR ET SUPPORT DE TRACHEOSTOME
Showing 12 of 57 declared devices.
Catalogue references include CBC0827, CBC1036, CBCF0836, CBCF1027, CNS0927, CNS1218.
European nomenclature codes declared: R010599, R010202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 57 |
| Country of registration | France |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 56 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | CEREDAS |
North American profile: Canada only. CEREDAS holds a Canadian licence but was not found in the U.S. register.