Single Use Infusion Pump - EUDAMED Registration 08800027705184

Access comprehensive regulatory information for Single Use Infusion Pump in the European Union medical device market through Pure Global AI's free database. This Class IIb device is registered with EU EUDAMED under Primary DI 08800027705184 and manufactured by S&S Med Co.,Ltd. in Republic of Korea.

This page provides complete registration details including trade name (CareVis BoluS), manufacturer information, authorized representative details, competent authority (Ministerie van Volksgezondheid, Welzijn en Sport), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.