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PRUEBA RÁPIDA PARA DETECCIÓN DE DENGUE - COFEPRIS Registration 0383R2022 SSA

Access comprehensive regulatory information for PRUEBA RÁPIDA PARA DETECCIÓN DE DENGUE (PRUEBA RÁPIDA PARA DETECCIÓN DE DENGUE) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 0383R2022 SSA and manufactured by DIINSEL, S.A. DE C.V.. The device was registered on May 17, 2022.

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
0383R2022 SSA
PRUEBA RÁPIDA PARA DETECCIÓN DE DENGUE
COFEPRIS Analysis ID: 0383R2022 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)
DIINSEL DENGUE IGG/IGM RAPID TEST DEVICE
Trade Name (English)
DIINSEL DENGUE IGG/IGM RAPID TEST DEVICE
Registration Information
Analysis ID
0383R2022 SSA
Registration Date
May 17, 2022
Manufacturer / Fabricante
Name (Spanish)
DIINSEL, S.A. DE C.V.
Name (English)
DIINSEL, S.A. DE C.V.