Defogger Anti-fog System - EUDAMED Registration 08809380052720

Access comprehensive regulatory information for Defogger Anti-fog System in the European Union medical device market through Pure Global AI's free database. This Class IIa device is registered with EU EUDAMED under Primary DI 08809380052720 and manufactured by The Standard. Co., Ltd. in Republic of Korea.

This page provides complete registration details including trade name (Defogger Anti-fog System), 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.