Mexico COFEPRIS registration 1049R2024 SSA

ENSAYO PARA LA DETERMINACIÓN CUANTITATIVA DE LA ALDOLASA (ALD)

EN: ENSAYO PARA LA DETERMINACIÓN CUANTITATIVA DE LA ALDOLASA (ALD)
Mexico flagMexico·Clase I·III. Agentes de diagnóstico·SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.·Registered April 15, 2024
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)
ALDOLASE
Trade Name (English)
ALDOLASE
Registration information
Analysis ID
1049R2024 SSA
Registration Date
April 15, 2024
Manufacturer / Fabricante
Name (English)
SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.
About this record

Access comprehensive regulatory information for ENSAYO PARA LA DETERMINACIÓN CUANTITATIVA DE LA ALDOLASA (ALD) (ENSAYO PARA LA DETERMINACIÓN CUANTITATIVA DE LA ALDOLASA (ALD)) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1049R2024 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.. The device was registered on April 15, 2024.

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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