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KIT DE PRUEBA PARA DETERMINACIONES IN VITRO (IVD) DE TESTOSTERONA TOTAL EN SUERO HUMANO - COFEPRIS Registration 1690R2022 SSA

Access comprehensive regulatory information for KIT DE PRUEBA PARA DETERMINACIONES IN VITRO (IVD) DE TESTOSTERONA TOTAL EN SUERO HUMANO (KIT DE PRUEBA PARA DETERMINACIONES IN VITRO (IVD) DE TESTOSTERONA TOTAL EN SUERO HUMANO) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1690R2022 SSA and manufactured by INOCHEM, S.A. DE C.V.. The device was registered on December 16, 2022.

This page provides complete registration details including product type (III. Agentes de diagn贸stico), 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
1690R2022 SSA
KIT DE PRUEBA PARA DETERMINACIONES IN VITRO (IVD) DE TESTOSTERONA TOTAL EN SUERO HUMANO
COFEPRIS Analysis ID: 1690R2022 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. Agentes de diagn贸stico
Product Type (English)
III. Agentes de diagn贸stico
Trade Name (Spanish)
TOTAL TESTOSTERONE ELISA
Trade Name (English)
TOTAL TESTOSTERONE ELISA
Registration Information
Analysis ID
1690R2022 SSA
Registration Date
December 16, 2022
Manufacturer / Fabricante
Name (Spanish)
INOCHEM, S.A. DE C.V.
Name (English)
INOCHEM, S.A. DE C.V.