EUDAMED last updated this device on Aug 14, 2026
QuikRead go wrCRP+Hb
B-06438115000990On the marketIVDD — General
- Applicable legislation
- —
- Organization name
- Aidian Oy
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 →- 06438115000990
- Reference / catalog number
- 146255
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.
QuikRead go wrCRP+Hb is an IVDD-legacy in vitro diagnostic registered in EUDAMED. It is classified as IVDD — General. Manufactured by Aidian Oy. Placed on the EU market in Finland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.