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D-100™ HEMOGLOBIN TESTING SYSTEM - COFEPRIS Registration 2031E2018 SSA

Access comprehensive regulatory information for D-100™ HEMOGLOBIN TESTING SYSTEM (D-100™ HEMOGLOBIN TESTING SYSTEM) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2031E2018 SSA and manufactured by BIO-RAD, S.A.. The device was registered on August 16, 2018.

This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), 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
2031E2018 SSA
D-100™ HEMOGLOBIN TESTING SYSTEM
COFEPRIS Analysis ID: 2031E2018 SSA
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Product Use / Uso del Producto
Spanish

EL D-100™ HEMOGLOBIN TESTING SYSTEM REALIZA ANÁLISIS AUTOMATIZADOS DE MUESTRAS DE SANGRE EN EL LABORATORIO CLÍNICO.

English

THE D-100™ HEMOGLOBIN TESTING SYSTEM PERFORMS AUTOMATED ANALYSIS OF BLOOD SAMPLES IN THE CLINICAL LABORATORY.

Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
I. EQUIPO MÉDICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
ANALIZADOR AUTOMÁTICO PARA DETERMINACIÓN DE HEMOGLOBINA
Trade Name (English)
AUTOMATIC ANALYZER FOR HEMOGLOBIN DETERMINATION
Registration Information
Analysis ID
2031E2018 SSA
Registration Date
August 16, 2018
Manufacturer / Fabricante
Name (Spanish)
BIO-RAD, S.A.
Name (English)
BIO-RAD, S.A.