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BIOMET GENERAL ACL/PCL INSTRUMENTS - COFEPRIS Registration 117E2019 SSA

Access comprehensive regulatory information for BIOMET GENERAL ACL/PCL INSTRUMENTS (BIOMET GENERAL ACL/PCL INSTRUMENTS) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 117E2019 SSA and manufactured by BIOMET Mร‰XICO, S.A. DE C.V.. The device was registered on January 29, 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.

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COFEPRIS Official Data
Clase II
117E2019 SSA
BIOMET GENERAL ACL/PCL INSTRUMENTS
COFEPRIS Analysis ID: 117E2019 SSA
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Product Use / Uso del Producto
Spanish

INSTRUMENTAL PARA EL APOYO EN CIRUGรAS DE RECONSTRUCCIร“N DEL LIGAMENTO CRUZADO ANTERIOR Y LIGAMENTO CRUZADO POSTERIOR

English

INSTRUMENTS FOR SUPPORT IN ANTERIOR CRUCIATE LIGAMENT AND POSTERIOR CRUCIATE LIGAMENT RECONSTRUCTION SURGERIES

Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
I. EQUIPO Mร‰DICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
INSTRUMENTAL PARA LCA/LCP
Trade Name (English)
INSTRUMENTAL PARA LCA/LCP
Registration Information
Analysis ID
117E2019 SSA
Registration Date
January 29, 2019
Manufacturer / Fabricante
Name (English)
BIOMET Mร‰XICO, S.A. DE C.V.