BIOMET GENERAL ACL/PCL INSTRUMENTS
INSTRUMENTAL PARA EL APOYO EN CIRUGÍAS DE RECONSTRUCCIÓN DEL LIGAMENTO CRUZADO ANTERIOR Y LIGAMENTO CRUZADO POSTERIOR
INSTRUMENTS FOR SUPPORT IN ANTERIOR CRUCIATE LIGAMENT AND POSTERIOR CRUCIATE LIGAMENT RECONSTRUCTION SURGERIES
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- I. EQUIPO MÉDICO
- Product Type (English)
- I. MEDICAL EQUIPMENT
- Trade Name (Spanish)
- INSTRUMENTAL PARA LCA/LCP
- Trade Name (English)
- INSTRUMENTAL PARA LCA/LCP
- Analysis ID
- 117E2019 SSA
- Registration Date
- January 29, 2019
- Name (Spanish)
- BIOMET MÉXICO, S.A. DE C.V.
- Name (English)
- BIOMET MÉXICO, S.A. DE C.V.
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 MÉXICO, 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.