INSTRUMENTAL PARA SISTEMA DE CABLE DE CERCLAJE CABLE-READY.
Mexico·Clase I·I. MEDICAL EQUIPMENT·BIOMET MÉXICO, S.A. DE C.V.·Registered March 15, 2019INDICADO PARA USO INTRAOPERATORIO EN LA REDUCCIÓN Y ESTABILIZACIÓN DE FRACTURAS Y PARA PREPARAR LA RECEPCIÓN DEL IMPLANTE EN EL SITIO DE MANUFACTURA.
INDICATED FOR INTRAOPERATIVE USE IN THE REDUCTION AND STABILIZATION OF FRACTURES AND TO PREPARE THE RECEPTION OF THE IMPLANT AT THE MANUFACTURING SITE.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- I. EQUIPO MÉDICO
- Product Type (English)
- I. MEDICAL EQUIPMENT
- Trade Name (Spanish)
- INSTRUMENTAL PARA SISTEMA DE CABLE DE CERCLAJE PARA FIJACIÓN ÓSEA.
- Trade Name (English)
- INSTRUMENTS FOR CERCLAGE CABLE SYSTEM FOR BONE FIXATION.
- Analysis ID
- 546E2019 SSA
- Registration Date
- March 15, 2019
- Name (Spanish)
- BIOMET MÉXICO, S.A. DE C.V.
- Name (English)
- BIOMET MÉXICO, S.A. DE C.V.
Access comprehensive regulatory information for INSTRUMENTAL PARA SISTEMA DE CABLE DE CERCLAJE CABLE-READY. (INSTRUMENTS FOR CABLE-READY CERCLAGE CABLE SYSTEM.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 546E2019 SSA and manufactured by BIOMET MÉXICO, S.A. DE C.V.. The device was registered on March 15, 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.