EUDAMED last updated this device on Aug 5, 2026
QUBE
955102834NBRPFRYB60FUOn the marketClass I
- Applicable legislation
- —
- Organization name
- Qube Medical Products Sdn Bhd
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 →- 09551028344610
- Reference / catalog number
- NBR12PFFT60RYBSC
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.
QUBE is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Qube Medical Products Sdn Bhd. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.