SISTEMA PARA LA FIJACIÓN DE TOBILLO Y PIE, OSSEOTI BIOMET
Mexico·Clase III·II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS·BIOMET MÉXICO, S.A. DE C.V.·Registered November 16, 2018EL SISTEMA PARA LA FIJACIÓN DE TOBILLO Y PIE, OSSEOTI BIOMET ESTÁ DISEÑADO PARA SU USO EN LA FIJACIÓN ÓSEA INTERNA DE ESTRUCTURAS ÓSEAS, FUSIONES U OSTEOTOMÍAS EN EL TOBILLO Y EL PIE, TALES COMO: • OSTEOTOMÍA DE ALARGAMIENTO DE EVANS. • ARTRODESIS DE LA
THE SYSTEM FOR ANKLE AND FOOT FIXATION, OSSEOTI BIOMET IS DESIGNED FOR USE IN INTERNAL BONE FIXATION OF BONE STRUCTURES, FUSIONS OR OSTEOTOMIES IN THE ANKLE AND FOOT, SUCH AS: • EVANS ELONGATION OSTEOTOMY. • ARTHRODESIS OF
- Risk Class / Clase de Riesgo
- Clase III
- Product Type (Spanish)
- II. PROTESIS, ÓRTESIS Y AYUDAS FUNCIONALES
- Product Type (English)
- II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS
- Trade Name (Spanish)
- SISTEMA PARA LA FIJACIÓN DE TOBILLO Y PIE
- Trade Name (English)
- SYSTEM FOR FIXING ANKLE AND FOOT
- Analysis ID
- 2637C2018 SSA
- Registration Date
- November 16, 2018
- Name (Spanish)
- BIOMET MÉXICO, S.A. DE C.V.
- Name (English)
- BIOMET MÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for SISTEMA PARA LA FIJACIÓN DE TOBILLO Y PIE, OSSEOTI BIOMET (ANKLE AND FOOT FIXATION SYSTEM, OSSEOTI BIOMET) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 2637C2018 SSA and manufactured by BIOMET MÉXICO, S.A. DE C.V.. The device was registered on November 16, 2018.
This page provides complete registration details including product type (II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS), 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.