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QUANTA FLASH® CALPROTECTIN EXTRACTION BUFFER - COFEPRIS Registration 1078R2019 SSA

Access comprehensive regulatory information for QUANTA FLASH® CALPROTECTIN EXTRACTION BUFFER (QUANTA FLASH® CALPROTECTIN EXTRACTION BUFFER) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1078R2019 SSA and manufactured by I.L. DIAGNOSTICS, S.A. DE C.V.. The device was registered on May 20, 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
1078R2019 SSA
QUANTA FLASH® CALPROTECTIN EXTRACTION BUFFER
COFEPRIS Analysis ID: 1078R2019 SSA
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Product Use / Uso del Producto
Spanish

EL QUANTA FLASH CALPROTECTIN EXTRACTION BUFFER ESTÁ DESTINADO A UTILIZARSE CON LOS REACTIVOS QUANTA FLASH CALPROTECTIN REAGENTS COMO SOLUCIÓN DE EXTRACCIÓN DE MUESTRAS

English

THE QUANTA FLASH CALPROTECTIN EXTRACTION BUFFER IS INTENDED FOR USE WITH QUANTA FLASH CALPROTECTIN REAGENTS AS A SAMPLE EXTRACTION SOLUTION

Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. AGENTES DE DIAGNÓSTICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
SOLUCION DE EXTRACCION DE MUESTRAS
Trade Name (English)
SAMPLE EXTRACTION SOLUTION
Registration Information
Analysis ID
1078R2019 SSA
Registration Date
May 20, 2019
Manufacturer / Fabricante
Name (English)
I.L. DIAGNOSTICS, S.A. DE C.V.