Mexico COFEPRIS registration 0317R2024 SSA

REACTIVO PARA LA DETERMINACIÓN CUANTITATIVA DE TSH EN SUERO, PLASMA O SANGRE TOTAL.

EN: REACTIVO PARA LA DETERMINACIÓN CUANTITATIVA DE TSH EN SUERO, PLASMA O SANGRE TOTAL.
Mexico flagMexico·Clase I·III. Agentes de diagnóstico·ATYDE MÉXICO S.A. DE C.V.·Registered January 30, 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)
THYROID STIMULATING HORMONE (TSH) TEST KIT (IMMUNOFLUORESCENCE) GENRUI.
Trade Name (English)
THYROID STIMULATING HORMONE (TSH) TEST KIT (IMMUNOFLUORESCENCE) GENRUI.
Registration information
Analysis ID
0317R2024 SSA
Registration Date
January 30, 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 TSH EN SUERO, PLASMA O SANGRE TOTAL. (REACTIVO PARA LA DETERMINACIÓN CUANTITATIVA DE TSH EN SUERO, PLASMA O SANGRE TOTAL.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0317R2024 SSA and manufactured by ATYDE MÉXICO S.A. DE C.V.. The device was registered on January 30, 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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