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HSV 1/2 IGM PRUEBA RÁPIDA EN SANGRE TOTAL, SUERO Y PLASMA - COFEPRIS Registration 0139R2024 SSA

Access comprehensive regulatory information for HSV 1/2 IGM PRUEBA RÁPIDA EN SANGRE TOTAL, SUERO Y PLASMA (HSV 1/2 IGM PRUEBA RÁPIDA EN SANGRE TOTAL, SUERO Y PLASMA) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 0139R2024 SSA and manufactured by QUIMIBIOL, S.A. DE C.V.. The device was registered on January 17, 2024.

This page provides complete registration details including product type (III. Agentes de diagnóstico), 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 II
0139R2024 SSA
HSV 1/2 IGM PRUEBA RÁPIDA EN SANGRE TOTAL, SUERO Y PLASMA
COFEPRIS Analysis ID: 0139R2024 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
III. Agentes de diagnóstico
Product Type (English)
III. Agentes de diagnóstico
Trade Name (Spanish)
MEXLAB BIO-TORCH
Trade Name (English)
MEXLAB BIO-TORCH
Registration Information
Analysis ID
0139R2024 SSA
Registration Date
January 17, 2024
Manufacturer / Fabricante
Name (English)
QUIMIBIOL, S.A. DE C.V.