CLEARVUE 350/550 - COFEPRIS Registration 305E2018 SSA

Access comprehensive regulatory information for CLEARVUE 350/550 (CLEARVUE 350/550) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 305E2018 SSA and manufactured by PHILIPS MÉXICO COMMERCIAL, S.A. DE C.V.. The device was registered on February 02, 2018.

This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.