EUDAMED last updated this device on Aug 13, 2026
Tissue-Tek Genie® Controller System
06152338226JAOn the marketIVDR Class A
- Applicable legislation
- —
- Organization name
- Sakura Finetek USA, Inc
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 →- 00615233002907
- Reference / catalog number
- 0008008-01
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.
Tissue-Tek Genie® Controller System is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Sakura Finetek USA, Inc. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.