Diamond S - EUDAMED Registration 05051977001304

Access comprehensive regulatory information for Diamond S in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI 05051977001304 and manufactured by Penlon Limited in United Kingdom (ex Northern Ireland).

This page provides complete registration details including trade name (Diamond S / Video Laryngoscope, Euro Plug, EN), manufacturer information, authorized representative details, competent authority (Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten/ Afdeling Gezondheidsproducten), 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.