EUDAMED last updated this device on Jul 7, 2026
LEGIONELLA BCYE + AB LAB-AGAR™
59026439APLEG_GVPCAGOn the marketIVDR Class A
- Applicable legislation
- —
- Organization name
- BioMaxima Spółka Akcyjna
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 →- 05902643929838
- Reference / catalog number
- PP 0178
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.
LEGIONELLA BCYE + AB LAB-AGAR™ is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by BioMaxima Spółka Akcyjna. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.