Cutaneous Electrode Pad - EUDAMED Registration 04719871185759

Access comprehensive regulatory information for Cutaneous Electrode Pad 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 04719871185759 and manufactured by Everyway Medical Instrument Co., Ltd. in Taiwan.

This page provides complete registration details including trade name (Everyway), 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.