SISTEMA SENTINEL FLEXIBLE REAMERS - COFEPRIS Registration 1097E2019 SSA

Access comprehensive regulatory information for SISTEMA SENTINEL FLEXIBLE REAMERS (SISTEMA SENTINEL FLEXIBLE REAMERS) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1097E2019 SSA and manufactured by BIOMET MÉXICO, S.A. DE C.V.. The device was registered on May 21, 2019.

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.