CLARITY ULTRA - COFEPRIS Registration 1219C2020 SSA

Access comprehensive regulatory information for CLARITY ULTRA (CLARITY ULTRA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1219C2020 SSA and manufactured by 3M MÉXICO, S.A. DE C.V.. The device was registered on September 10, 2020.

This page provides complete registration details including product type (IV. DENTAL SUPPLIES), 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.