Mexico COFEPRIS registration 1577R2022 SSA

REACTIVO PARA LA DETERMINACIÓN CUANTITATIVA DE FERRITINA

EN: REACTIVO PARA LA DETERMINACIÓN CUANTITATIVA DE FERRITINA
Mexico flagMexico·Clase I·III. Agentes de diagnóstico·LAB-CENTER DE MÉXICO S.A. DE C.V.·Registered December 14, 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)
FERR-TURBI
Trade Name (English)
FERR-TURBI
Registration information
Analysis ID
1577R2022 SSA
Registration Date
December 14, 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 CUANTITATIVA DE FERRITINA (REACTIVO PARA LA DETERMINACIÓN CUANTITATIVA DE FERRITINA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1577R2022 SSA and manufactured by LAB-CENTER DE MÉXICO S.A. DE C.V.. The device was registered on December 14, 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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