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REFRACTÓMETRO/QUERATOMETRO OPD-SCAN II NIDEK - COFEPRIS Registration 1070E2019 SSA

Access comprehensive regulatory information for REFRACTÓMETRO/QUERATOMETRO OPD-SCAN II NIDEK (REFRACTÓMETRO/QUERATOMETRO OPD-SCAN II NIDEK) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1070E2019 SSA and manufactured by S4OPTIK, S.A. DE C.V.. The device was registered on May 20, 2019.

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
1070E2019 SSA
REFRACTÓMETRO/QUERATOMETRO OPD-SCAN II NIDEK
COFEPRIS Analysis ID: 1070E2019 SSA
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Product Use / Uso del Producto
Spanish

EL REFRACTÓMETRO/QUERATÓMETRO, QUE TIENE TANTO LA FUNCIÓN DE MEDICIÓN DE ERROR REFRACTIVO OBJETIVO Y LA FUNCIÓN DE ANÁLISIS CORNEAL (TOPOGRAFÍA), PARA MAPEO DE LA DISTRIBUCIÓN DE PODER DE REFRACCIÓN DEL OJO POR MEDIO DE LA MEDICIÓN Y EL ANÁLISIS DE LA PO

English

THE REFRACTOMETER/KERATOMETER, WHICH HAS BOTH THE OBJECTIVE REFRACTIVE ERROR MEASUREMENT FUNCTION AND THE CORNEAL ANALYSIS (TOPOGRAPHY) FUNCTION, FOR MAPPING THE REFRACTIVE POWER DISTRIBUTION OF THE EYE BY MEANS OF PO MEASUREMENT AND ANALYSIS.

Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
I. EQUIPO MÉDICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
REFRACTÓMETRO/QUERATOMETRO
Trade Name (English)
REFRACTOMETER/KERATOMETER
Registration Information
Analysis ID
1070E2019 SSA
Registration Date
May 20, 2019
Manufacturer / Fabricante
Name (Spanish)
S4OPTIK, S.A. DE C.V.
Name (English)
S4OPTIK, S.A. DE C.V.