EEG Green Reference Lead - EUDAMED Registration 10850037993243
Access comprehensive regulatory information for EEG Green Reference Lead 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 10850037993243 and manufactured by MECTA LLC in United States.
This page provides complete registration details including 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.
ELECTROCONVULSIVE THERAPY (ECT) EQUIPMENT

