EUDAMED last updated this device on Aug 5, 2026
SG313 4
697628156RP5L- Applicable legislation
- —
- Organization name
- FuQuan Toboom Technologies 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 →- 06976281567706
- Reference / catalog number
- SG313 4
SG313 4 is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by FuQuan Toboom Technologies Co., Ltd. Placed on the EU market in Sweden. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.