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FLEXIGRAFT - COFEPRIS Registration 1587C2019 SSA

Access comprehensive regulatory information for FLEXIGRAFT (FLEXIGRAFT) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1587C2019 SSA and manufactured by EMERGO S DE RL DE CV. The device was registered on August 12, 2019.

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.

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COFEPRIS Official Data
Clase III
1587C2019 SSA
FLEXIGRAFT
COFEPRIS Analysis ID: 1587C2019 SSA
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Product Use / Uso del Producto
Spanish

BIOIMPLANTE DE ALOINJERTO DE LIGAMENTO Y TENDON

English

BIOIMPLANT OF LIGAMENT AND TENDON ALLOGRAFT

Device Classification
Risk Class / Clase de Riesgo
Clase III
Product Type (Spanish)
II. PROTESIS, ร“RTESIS Y AYUDAS FUNCIONALES
Product Type (English)
II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS
Trade Name (Spanish)
BIOIMPLANTE DE ALOINJERTO DE LIGAMENTO Y TENDON
Trade Name (English)
BIOIMPLANT OF LIGAMENT AND TENDON ALLOGRAFT
Registration Information
Analysis ID
1587C2019 SSA
Registration Date
August 12, 2019
Manufacturer / Fabricante
Name (Spanish)
EMERGO S DE RL DE CV
Name (English)
EMERGO S DE RL DE CV