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ANCLAJE DE SUTURA PARA HOMBRO - COFEPRIS Registration 0492C2024 SSA

Access comprehensive regulatory information for ANCLAJE DE SUTURA PARA HOMBRO (ANCLAJE DE SUTURA PARA HOMBRO) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 0492C2024 SSA and manufactured by SMITH & NEPHEW, S.A. DE C.V.. The device was registered on February 12, 2024.

This page provides complete registration details including product type (II. Protesis, รณrtesis 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
0492C2024 SSA
ANCLAJE DE SUTURA PARA HOMBRO
COFEPRIS Analysis ID: 0492C2024 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase III
Product Type (Spanish)
II. Protesis, รณrtesis y ayudas funcionales
Product Type (English)
II. Protesis, รณrtesis y ayudas funcionales
Trade Name (Spanish)
ANCLAJE DE SUTURA REGENESORBโ„ข SIN NUDOS HEALICOIL
Trade Name (English)
ANCLAJE DE SUTURA REGENESORBโ„ข SIN NUDOS HEALICOIL
Registration Information
Analysis ID
0492C2024 SSA
Registration Date
February 12, 2024
Manufacturer / Fabricante
Name (English)
SMITH & NEPHEW, S.A. DE C.V.