EUDAMED last updated this device on Jul 23, 2026
Anti-Fya for card method Coombs-reactive, polyclonal, human
B-04250861815534On the marketIVDD — Annex II List B
- Applicable legislation
- —
- Organization name
- ANTITOXIN GmbH
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 →- 04250861815534
- Reference / catalog number
- 02.182-03
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.
Anti-Fya for card method Coombs-reactive, polyclonal, human is an IVDD-legacy in vitro diagnostic registered in EUDAMED. It is classified as IVDD — Annex II List B. Manufactured by ANTITOXIN GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.