EUDAMED last updated this device on Aug 29, 2026
SDB2110
697655656NEEDLESDB2110H3On the marketClass IIa
- Applicable legislation
- —
- Organization name
- Weihai Sunway Medical Technology 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 →- 06976556561637
- Reference / catalog number
- SDB2110
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.
SDB2110 is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Weihai Sunway Medical Technology Co.,Ltd. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.