Mexico COFEPRIS registration 0313R2024 SSA

REACTIVO PARA LA DETERMINACIÓN CUANTITATIVA DE TIROXINA T4 EN SUERO HUMANO, PLASMA O SANGRE ENTERA.

EN: REACTIVO PARA LA DETERMINACIÓN CUANTITATIVA DE TIROXINA T4 EN SUERO HUMANO, PLASMA O SANGRE ENTERA.
Mexico flagMexico·Clase I·III. Agentes de diagnóstico·ATYDE MÉXICO S.A. DE C.V.·Registered January 29, 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)
THYROXINE (T4) TEST KIT (IMMUNOFLUORESCENCE) GENRUI.
Trade Name (English)
THYROXINE (T4) TEST KIT (IMMUNOFLUORESCENCE) GENRUI.
Registration information
Analysis ID
0313R2024 SSA
Registration Date
January 29, 2024
Manufacturer / Fabricante
Name (English)
ATYDE MÉXICO S.A. DE C.V.
About this record

Access comprehensive regulatory information for REACTIVO PARA LA DETERMINACIÓN CUANTITATIVA DE TIROXINA T4 EN SUERO HUMANO, PLASMA O SANGRE ENTERA. (REACTIVO PARA LA DETERMINACIÓN CUANTITATIVA DE TIROXINA T4 EN SUERO HUMANO, PLASMA O SANGRE ENTERA.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0313R2024 SSA and manufactured by ATYDE MÉXICO S.A. DE C.V.. The device was registered on January 29, 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.

Free DatabasePowered by Pure Global AICOFEPRIS Official DataClase I