INSTRUMENTAL QUIRÚRGICO PARA LA COLOCACIÓN DEL SISTEMA DE FIJACIÓN DE TOBILLO Y PIE, OSSEOTI BIOMET. - COFEPRIS Registration 2642E2018 SSA
Access comprehensive regulatory information for INSTRUMENTAL QUIRÚRGICO PARA LA COLOCACIÓN DEL SISTEMA DE FIJACIÓN DE TOBILLO Y PIE, OSSEOTI BIOMET. (SURGICAL INSTRUMENTS FOR THE PLACEMENT OF THE ANKLE AND FOOT FIXATION SYSTEM, OSSEOTI BIOMET.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2642E2018 SSA and manufactured by BIOMET MÉXICO, S.A. DE C.V.. The device was registered on November 20, 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.
INSTRUMENTAL QUIRÚRGICO PARA LA COLOCACIÓN DEL SISTEMA DE FIJACIÓN DE TOBILLO Y PIE, OSSEOTI BIOMET ESTÁ INDICADO PARA REALIZAR PROCEDIMIENTOS QUIRÚRGICOS DE IMPLANTACIÓN, ESTABILIZACIÓN, REVISIÓN, COLOCACIÓN Y/O AUXILIAR EN PROCEDIMIENTOS QUIRÚRGICOS EN
SURGICAL INSTRUMENTS FOR THE PLACEMENT OF THE ANKLE AND FOOT FIXATION SYSTEM, OSSEOTI BIOMET IS INDICATED TO PERFORM SURGICAL PROCEDURES OF IMPLANTATION, STABILIZATION, REVISION, PLACEMENT AND / OR AUXILIARY IN SURGICAL PROCEDURES IN