LOGIQ Fortis - EUDAMED Registration 00195278877130
Access comprehensive regulatory information for LOGIQ Fortis 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 00195278877130 and manufactured by GE Ultrasound Korea Ltd in Republic of Korea.
This page provides complete registration details including manufacturer information, authorized representative details, competent authority (Agence Nationale de Sรฉcuritรฉ du Mรฉdicament et des Produits de Santรฉ), 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.
INTERNAL ULTRASOUND SCANNERS

