EUDAMED last updated this device on Aug 5, 2026
KIT SURGICAL EPIKUT
999520000072K7On the marketClass IIa
- Applicable legislation
- —
- Organization name
- S.I.N. Implant System Ltda.
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 →- 07899995272867
- Reference / catalog number
- KCSE 02
Regulatory classification unavailableThis product's Basic UDI record hasn't been published in EUDAMED yet. Classification and compliance details will appear automatically once EUDAMED publishes it.
KIT SURGICAL EPIKUT is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by S.I.N. Implant System Ltda.. Placed on the EU market in Portugal. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.