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JERINGA PRELLENADA CON ÁCIDO HIALURÓNICO E HIDROXIAPATITA - COFEPRIS Registration 0401C2024 SSA

Access comprehensive regulatory information for JERINGA PRELLENADA CON ÁCIDO HIALURÓNICO E HIDROXIAPATITA (JERINGA PRELLENADA CON ÁCIDO HIALURÓNICO E HIDROXIAPATITA) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 0401C2024 SSA and manufactured by MANDALA MÉXICO LEGAL AFFAIRS, S.A. DE C.V.. The device was registered on February 06, 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
0401C2024 SSA
JERINGA PRELLENADA CON ÁCIDO HIALURÓNICO E HIDROXIAPATITA
COFEPRIS Analysis ID: 0401C2024 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)
NEAUVIA STIMULATE
Trade Name (English)
NEAUVIA STIMULATE
Registration Information
Analysis ID
0401C2024 SSA
Registration Date
February 06, 2024
Manufacturer / Fabricante
Name (English)
MANDALA MÉXICO LEGAL AFFAIRS, S.A. DE C.V.