Mexico COFEPRIS registration 0874R2024 SSA

TIRAS DE PRUEBA DE ADULTERACIÓN DE ORINA.

EN: TIRAS DE PRUEBA DE ADULTERACIÓN DE ORINA.
Mexico flagMexico·Clase I·III. Agentes de diagnóstico·DIINSEL, S.A. DE C.V.·Registered March 26, 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)
D-CHECK UROANALISIS.
Trade Name (English)
D-CHECK UROANALISIS.
Registration information
Analysis ID
0874R2024 SSA
Registration Date
March 26, 2024
Manufacturer / Fabricante
Name (Spanish)
DIINSEL, S.A. DE C.V.
Name (English)
DIINSEL, S.A. DE C.V.
About this record

Access comprehensive regulatory information for TIRAS DE PRUEBA DE ADULTERACIÓN DE ORINA. (TIRAS DE PRUEBA DE ADULTERACIÓN DE ORINA.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0874R2024 SSA and manufactured by DIINSEL, S.A. DE C.V.. The device was registered on March 26, 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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