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ASCA-IGG/IGA - COFEPRIS Registration 1194R2019 SSA

Access comprehensive regulatory information for ASCA-IGG/IGA (ASCA-IGG/IGA) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1194R2019 SSA and manufactured by BIO SIMEX, S.A. DE C.V.. The device was registered on May 31, 2019.

This page provides complete registration details including product type (III. DIAGNOSTIC AGENTS), 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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COFEPRIS Official Data
Clase II
1194R2019 SSA
ASCA-IGG/IGA
COFEPRIS Analysis ID: 1194R2019 SSA
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Product Use / Uso del Producto
Spanish

REACTIVOS PARA LA DETERMINACIร“N CUALITATIVA Y CUANTITATIVA DE ASCA-IGG/IGA EN SUERO O PLASMA HUMANOS.

English

REAGENTS FOR THE QUALITATIVE AND QUANTITATIVE DETERMINATION OF ASCA-IGG/IGA IN HUMAN SERUM OR PLASMA.

Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
III. AGENTES DE DIAGNร“STICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
REACTIVO PARA LA DETERMINACIร“N DE ASCA-IGG/IGA
Trade Name (English)
REAGENT FOR THE DETERMINATION OF ASCA-IGG/IGA
Registration Information
Analysis ID
1194R2019 SSA
Registration Date
May 31, 2019
Manufacturer / Fabricante
Name (English)
BIO SIMEX, S.A. DE C.V.