HemosIL CL Anti-Cardiolipin IgM - EUDAMED Registration 08426951011193

Access comprehensive regulatory information for HemosIL CL Anti-Cardiolipin IgM in the European Union medical device market through Pure Global AI's free database. This Class B device is registered with EU EUDAMED under Primary DI 08426951011193 and manufactured by Instrumentation Laboratory Company in United States.

This page provides complete registration details including trade name (HemosIL CL Anti-Cardiolipin IgM), manufacturer information, authorized representative details, competent authority (Ministero della salute - Direzione generale dei dispositivi medici e del servizio farmaceutico), 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.