Mexico COFEPRIS registration 1152R2022 SSA

REACTIVO PARA LA DETERMINACIÓN DE LACTATO DESHIDROGENASA

EN: REACTIVO PARA LA DETERMINACIÓN DE LACTATO DESHIDROGENASA
Mexico flagMexico·Clase I·III. Agentes de diagnóstico·LAB-CENTER DE MÉXICO S.A. DE C.V.·Registered October 21, 2022
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)
LDH
Trade Name (English)
LDH
Registration information
Analysis ID
1152R2022 SSA
Registration Date
October 21, 2022
Manufacturer / Fabricante
Name (English)
LAB-CENTER DE MÉXICO S.A. DE C.V.
About this record

Access comprehensive regulatory information for REACTIVO PARA LA DETERMINACIÓN DE LACTATO DESHIDROGENASA (REACTIVO PARA LA DETERMINACIÓN DE LACTATO DESHIDROGENASA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1152R2022 SSA and manufactured by LAB-CENTER DE MÉXICO S.A. DE C.V.. The device was registered on October 21, 2022.

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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