EUDAMED last updated this device on Feb 22, 2024
CESSYS® FHD Cervical Hybrid Scope, combo
B-04250337105879- Applicable legislation
- —
- Organization name
- Joimax GmbH
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →- 04250337105879
- Reference / catalog number
- CH402100C
CESSYS® FHD Cervical Hybrid Scope, combo is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Joimax GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.