EUDAMED last updated this device on May 26, 2026
Aqvitox® - D gél
8588007405AQVITOXDGEL49On the marketClass IIb
- Applicable legislation
- —
- Organization name
- Aqvitox Technology, s.r.o.
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 →- 08588007405650
- Reference / catalog number
- 40 ml
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.
Aqvitox® - D gél is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Aqvitox Technology, s.r.o.. Placed on the EU market in Slovakia. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.