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BIOIMPLANTE DE ALOINJERTO (FIBRAS MOLDEABLES DESMINERALIZADAS) - COFEPRIS Registration 0663C2024 SSA

Access comprehensive regulatory information for BIOIMPLANTE DE ALOINJERTO (FIBRAS MOLDEABLES DESMINERALIZADAS) (BIOIMPLANTE DE ALOINJERTO (FIBRAS MOLDEABLES DESMINERALIZADAS)) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 0663C2024 SSA and manufactured by EMERGO S. DE R.L. DE C.V.. The device was registered on March 07, 2024.

This page provides complete registration details including product type (II. Protesis, 贸rtesis y ayudas funcionales), 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
0663C2024 SSA
BIOIMPLANTE DE ALOINJERTO (FIBRAS MOLDEABLES DESMINERALIZADAS)
COFEPRIS Analysis ID: 0663C2024 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase III
Product Type (Spanish)
II. Protesis, 贸rtesis y ayudas funcionales
Product Type (English)
II. Protesis, 贸rtesis y ayudas funcionales
Trade Name (Spanish)
PLIAFX庐
Trade Name (English)
PLIAFX庐
Registration Information
Analysis ID
0663C2024 SSA
Registration Date
March 07, 2024
Manufacturer / Fabricante
Name (English)
EMERGO S. DE R.L. DE C.V.