EUDAMED last updated this device on Aug 7, 2026

SPEEDYBELL

B-08033860017767
On the marketClass IIa
Applicable legislation
Organization name
BIOPSYBELL SRL
08033860017767
Reference / catalog number
SB2107EC
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.

SPEEDYBELL is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by BIOPSYBELL SRL. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.