ClearLLab LS Lymphoid Screen Reagent - EUDAMED Registration 15099590686567

Access comprehensive regulatory information for ClearLLab LS Lymphoid Screen Reagent in the European Union medical device market through Pure Global AI's free database. This Class C device is registered with EU EUDAMED under Primary DI 15099590686567 and manufactured by Beckman Coulter India Private Limited in India.

This page provides complete registration details including trade name (ClearLLab LS Lymphoid Screen Reagent), manufacturer information, authorized representative details, competent authority (Health Products Regulatory Authority, Medical Devices Department), 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.