514/810nm LIO - EUDAMED Registration 05055272720328

Access comprehensive regulatory information for 514/810nm LIO 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 05055272720328 and manufactured by Keeler Ltd in United Kingdom (ex Northern Ireland).

This page provides complete registration details including trade name (514/810nm LIO), manufacturer information, authorized representative details, competent authority (Agencia Española de Medicamentos y Productos Sanitarios), 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.