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ALINITY C CERULOPLASMIN - COFEPRIS Registration 95R2019 SSA

Access comprehensive regulatory information for ALINITY C CERULOPLASMIN (ALINITY C CERULOPLASMIN) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 95R2019 SSA and manufactured by ABBOTT LABORATORIES DE MEXICO SA DE CV. The device was registered on January 28, 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 I
95R2019 SSA
ALINITY C CERULOPLASMIN
COFEPRIS Analysis ID: 95R2019 SSA
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Product Use / Uso del Producto
Spanish

ENSAYO PARA LA DETERMINACION DE CERUPLASMINA

English

ASSAY FOR THE DETERMINATION OF CERUPLASMIN

Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. AGENTES DE DIAGNร“STICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
ENSAYO PARA LA DETERMINACION DE CERUPLASMINA
Trade Name (English)
ASSAY FOR THE DETERMINATION OF CERUPLASMIN
Registration Information
Analysis ID
95R2019 SSA
Registration Date
January 28, 2019
Manufacturer / Fabricante
Name (English)
ABBOTT LABORATORIES DE MEXICO SA DE CV