EUDAMED last updated this device on Aug 28, 2026
DB2519F
697655656NEEDLEDB2519F5UOn 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 →- 06976556561224
- Reference / catalog number
- DB2519F
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.
DB2519F 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.