KELLER FUNNEL - EUDAMED Registration 10888628043725

Access comprehensive regulatory information for KELLER FUNNEL in the European Union medical device market through Pure Global AI's free database. This Class IIa device is registered with EU EUDAMED under Primary DI 10888628043725 and manufactured by Allergan Sales, LLC in United States.

This page provides complete registration details including trade name (Keller Funnel 2), 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.