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ANCLAJE PARA FIJACIÓN - COFEPRIS Registration 0427C2024 SSA

Access comprehensive regulatory information for ANCLAJE PARA FIJACIÓN (ANCLAJE PARA FIJACIÓN) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 0427C2024 SSA and manufactured by SMITH & NEPHEW, S.A. DE C.V.. The device was registered on February 07, 2024.

This page provides complete registration details including product type (II. Protesis, órtesis 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
0427C2024 SSA
ANCLAJE PARA FIJACIÓN
COFEPRIS Analysis ID: 0427C2024 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase III
Product Type (Spanish)
II. Protesis, órtesis y ayudas funcionales
Product Type (English)
II. Protesis, órtesis y ayudas funcionales
Trade Name (Spanish)
TWINFIX™ ULTRA TI
Trade Name (English)
TWINFIX™ ULTRA TI
Registration Information
Analysis ID
0427C2024 SSA
Registration Date
February 07, 2024
Manufacturer / Fabricante
Name (English)
SMITH & NEPHEW, S.A. DE C.V.