Limelight - EUDAMED Registration 00816722022110

Access comprehensive regulatory information for Limelight 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 00816722022110 and manufactured by Cutera, Inc. in United States.

This page provides complete registration details including trade name (Limelight), manufacturer information, authorized representative details, competent authority (DE/CA09 - Staatliches Gewerbeaufsichtsamt Hannover), 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.