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MINI TEST® HCG10 BIOSYNEX - COFEPRIS Registration 2297R2018 SSA

Access comprehensive regulatory information for MINI TEST® HCG10 BIOSYNEX (MINI TEST® HCG10 BIOSYNEX) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2297R2018 SSA and manufactured by PHARMACUR, S.A. DE C.V.. The device was registered on October 03, 2018.

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
2297R2018 SSA
MINI TEST® HCG10 BIOSYNEX
COFEPRIS Analysis ID: 2297R2018 SSA
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Product Use / Uso del Producto
Spanish

PRUEBA RÁPIDA PARA LA DETECCIÓN TEMPARANA DEL EMBARAZO.

English

RAPID TEST FOR EARLY DETECTION OF PREGNANCY.

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)
PRUEBA RÁPIDA PARA LA DETECCIÓN TEMPRANA DEL EMBARAZO
Trade Name (English)
RAPID TEST FOR EARLY DETECTION OF PREGNANCY
Registration Information
Analysis ID
2297R2018 SSA
Registration Date
October 03, 2018
Manufacturer / Fabricante
Name (English)
PHARMACUR, S.A. DE C.V.