Mexico COFEPRIS registration 1734E2021 SSA

ANALIZADORES LAURA

EN: LAURA ANALYZERS
Mexico flagMexico·Clase I·I. MEDICAL EQUIPMENT·HRD HIGHRESOLUTION DIAGNOSTICS, S.A. DEC.V.·Registered March 11, 2021
Product Use / Uso del Producto
Spanish

ANALIZADORES DISEÑADOS PARA LAEVALUACIÓN IN VITRO DE MUESTRAS DEORINA CON TIRAS DE DIAGNÓSTICO PHANMEDIANTE FOTOMETRÍA DE REFLACTANCIA,ASÍ COMO PARA LA EVALUACIÓN DESEDIMENTOS DE ORINA. PARA USO ENLABORATORIOS CLÍNICOS O DE GABINETE.

English

ANALYSERS DESIGNED FOR THE IN VITRO EVALUATION OF URINE SAMPLES WITH PHAN DIAGNOSTIC STRIPS BY REFLECTIVE PHOTOMETRY, AS WELL AS FOR THE EVALUATION OF URINE SEDIMENTS. FOR USE IN CLINICAL OR CABINET LABORATORIES.

Device classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
I. EQUIPO MÉDICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
ANALIZADORES DE ORINA
Trade Name (English)
URINE ANALYZERS
Registration information
Analysis ID
1734E2021 SSA
Registration Date
March 11, 2021
Manufacturer / Fabricante
Name (English)
HRD HIGHRESOLUTION DIAGNOSTICS, S.A. DEC.V.
About this record

Access comprehensive regulatory information for ANALIZADORES LAURA (LAURA ANALYZERS) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1734E2021 SSA and manufactured by HRD HIGHRESOLUTION DIAGNOSTICS, S.A. DEC.V.. The device was registered on March 11, 2021.

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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