Mexico COFEPRIS registration 1026E2022 SSA

ANALIZADOR CUANTITATIVO DE INMUNOFLUORESCENCIA

EN: ANALIZADOR CUANTITATIVO DE INMUNOFLUORESCENCIA
Mexico flagMexico·Clase I·I. Equipo Médico·AXMILAB, S.A. DE C.V.·Registered October 07, 2022
Device classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
I. Equipo Médico
Product Type (English)
I. Equipo Médico
Trade Name (Spanish)
DCR1000
Trade Name (English)
DCR1000
Registration information
Analysis ID
1026E2022 SSA
Registration Date
October 07, 2022
Manufacturer / Fabricante
Name (Spanish)
AXMILAB, S.A. DE C.V.
Name (English)
AXMILAB, S.A. DE C.V.
About this record

Access comprehensive regulatory information for ANALIZADOR CUANTITATIVO DE INMUNOFLUORESCENCIA (ANALIZADOR CUANTITATIVO DE INMUNOFLUORESCENCIA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1026E2022 SSA and manufactured by AXMILAB, S.A. DE C.V.. The device was registered on October 07, 2022.

This page provides complete registration details including product type (I. Equipo Médico), 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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