Mexico COFEPRIS registration 1153R2024 SSA

PRUEBA PARA LA DETERMINACIÓN CUANTITATIVA DE LA TRIYODOTIRONINA TOTAL (TT3) CIRCULANTE EN SUERO O PL

EN: PRUEBA PARA LA DETERMINACIÓN CUANTITATIVA DE LA TRIYODOTIRONINA TOTAL (TT3) CIRCULANTE EN SUERO O PL
Mexico flagMexico·Clase I·III. Agentes de diagnóstico·DRPRO MED S.A. DE C.V.·Registered April 22, 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)
TOTAL TRIIODOTHYRONINE (CLIA) - WONDFO.
Trade Name (English)
TOTAL TRIIODOTHYRONINE (CLIA) - WONDFO.
Registration information
Analysis ID
1153R2024 SSA
Registration Date
April 22, 2024
Manufacturer / Fabricante
Name (English)
DRPRO MED S.A. DE C.V.
About this record

Access comprehensive regulatory information for PRUEBA PARA LA DETERMINACIÓN CUANTITATIVA DE LA TRIYODOTIRONINA TOTAL (TT3) CIRCULANTE EN SUERO O PL (PRUEBA PARA LA DETERMINACIÓN CUANTITATIVA DE LA TRIYODOTIRONINA TOTAL (TT3) CIRCULANTE EN SUERO O PL) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1153R2024 SSA and manufactured by DRPRO MED S.A. DE C.V.. The device was registered on April 22, 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