EUDAMED last updated this device on Sep 17, 2026
Flowflex
B-6977L03164035T9On the marketIVDD — General
- Applicable legislation
- —
- Organization name
- Acon Biotech (Hangzhou) Co., Ltd.
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-6977L03164035T9
- Reference / catalog number
- L031-64035
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.
Flowflex is an IVDD-legacy in vitro diagnostic registered in EUDAMED. It is classified as IVDD — General. Manufactured by Acon Biotech (Hangzhou) Co., Ltd.. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.