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T3 ELISA CALBIOTECH - COFEPRIS Registration 1723R2019 SSA

Access comprehensive regulatory information for T3 ELISA CALBIOTECH (T3 ELISA CALBIOTECH) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1723R2019 SSA and manufactured by QUIMIBIOL, S.A. DE C.V.. The device was registered on August 26, 2019.

This page provides complete registration details including product type (III. DIAGNOSTIC AGENTS), 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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COFEPRIS Official Data
Clase I
1723R2019 SSA
T3 ELISA CALBIOTECH
COFEPRIS Analysis ID: 1723R2019 SSA
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Product Use / Uso del Producto
Spanish

INMUNOENSAYO PARA LA DETERMINACIร“N CUANTITATIVA DE TRIIODOTIRONINA (T3) EN SUERO HUMANO.

English

IMMUNOASSAY FOR THE QUANTITATIVE DETERMINATION OF TRIIODOTHYRONINE (T3) IN HUMAN SERUM.

Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. AGENTES DE DIAGNร“STICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
PRUEBA PARA DETERMINAR TRIIODOTIRONINA T3
Trade Name (English)
TEST TO DETERMINE TRIIODOTHYRONINE T3
Registration Information
Analysis ID
1723R2019 SSA
Registration Date
August 26, 2019
Manufacturer / Fabricante
Name (English)
QUIMIBIOL, S.A. DE C.V.