Mexico COFEPRIS registration 1398R2022 SSA

PRUEBA PARA LA DETERMINACIÓN DE CALPROTECTINA FECAL

EN: PRUEBA PARA LA DETERMINACIÓN DE CALPROTECTINA FECAL
Mexico flagMexico·Clase I·III. Agentes de diagnóstico·PRODUCTOS ROCHE, S.A. DE C.V.·Registered November 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)
FCAL TURBO
Trade Name (English)
FCAL TURBO
Registration information
Analysis ID
1398R2022 SSA
Registration Date
November 14, 2022
Manufacturer / Fabricante
Name (English)
PRODUCTOS ROCHE, S.A. DE C.V.
About this record

Access comprehensive regulatory information for PRUEBA PARA LA DETERMINACIÓN DE CALPROTECTINA FECAL (PRUEBA PARA LA DETERMINACIÓN DE CALPROTECTINA FECAL) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1398R2022 SSA and manufactured by PRODUCTOS ROCHE, S.A. DE C.V.. The device was registered on November 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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