Mexico COFEPRIS registration 0034R2024 SSA

CONTROL DE CALIDAD PARA PRUEBA DE DIAGNÓSTICO IN VITRO.

EN: CONTROL DE CALIDAD PARA PRUEBA DE DIAGNÓSTICO IN VITRO.
Mexico flagMexico·Clase I·III. Agentes de diagnóstico·KANA UNDESA, S.A. DE C.V.·Registered January 08, 2024
Device classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. Agentes de diagnóstico
Product Type (English)
III. Agentes de diagnóstico
Trade Name (Spanish)
STANDARD™ DENGUE NS1 AG CONTROL.
Trade Name (English)
STANDARD™ DENGUE NS1 AG CONTROL.
Registration information
Analysis ID
0034R2024 SSA
Registration Date
January 08, 2024
Manufacturer / Fabricante
Name (English)
KANA UNDESA, S.A. DE C.V.
About this record

Access comprehensive regulatory information for CONTROL DE CALIDAD PARA PRUEBA DE DIAGNÓSTICO IN VITRO. (CONTROL DE CALIDAD PARA PRUEBA DE DIAGNÓSTICO IN VITRO.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0034R2024 SSA and manufactured by KANA UNDESA, S.A. DE C.V.. The device was registered on January 08, 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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