EUDAMED last updated this device on Jun 2, 2026
Dr.Max+
B-888060-1EROn the marketIVDD — Self-testing
- Applicable legislation
- —
- Organization name
- PRIMA Lab SA
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 →- D-888060-1ER
- Reference / catalog number
- 888060-1CRS
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.
Dr.Max+ is an IVDD-legacy in vitro diagnostic registered in EUDAMED. It is classified as IVDD — Self-testing. Manufactured by PRIMA Lab SA. Placed on the EU market in Czechia. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.