EUDAMED last updated this device on Aug 14, 2026
AMNIOQUICK DUO+
B-03532678599724On the marketIVDD — General
- Applicable legislation
- —
- Organization name
- BIOSYNEX
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 →- 03532678599724
- Reference / catalog number
- 1090004
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.
AMNIOQUICK DUO+ is an IVDD-legacy in vitro diagnostic registered in EUDAMED. It is classified as IVDD — General. Manufactured by BIOSYNEX. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.