EUDAMED last updated this device on Aug 5, 2026
KIT ROTARY EXPANDER
999520000085KG- 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 →- 07899995209290
- Reference / catalog number
- KER
KIT ROTARY EXPANDER 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.