spECTrum Patient Stimulus Cable (replacement) - EUDAMED Registration 00850045508319

Access comprehensive regulatory information for spECTrum Patient Stimulus Cable (replacement) 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 00850045508319 and manufactured by SigmaStim Domestic 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.