EUDAMED last updated this device on Jul 23, 2026
GLUCOSE REAGENT KIT(HEXOKINASE METHOD)
B-06942202259890- Applicable legislation
- —
- Organization name
- DIRUI INDUSTRIAL CO., LTD
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 →- 06942202259890
- Reference / catalog number
- 232011802010
GLUCOSE REAGENT KIT(HEXOKINASE METHOD) is an IVDD-legacy in vitro diagnostic registered in EUDAMED. It is classified as IVDD — General. Manufactured by DIRUI INDUSTRIAL CO., LTD. Placed on the EU market in Austria. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.