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TOMÓGRAFO DE COHERENCIA ÓPTICA - COFEPRIS Registration 0713E2024 SSA

Access comprehensive regulatory information for TOMÓGRAFO DE COHERENCIA ÓPTICA (TOMÓGRAFO DE COHERENCIA ÓPTICA) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 0713E2024 SSA and manufactured by S4OPTIK, S.A. DE C.V.. The device was registered on March 13, 2024.

This page provides complete registration details including product type (I. Equipo Médico), 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 II
0713E2024 SSA
TOMÓGRAFO DE COHERENCIA ÓPTICA
COFEPRIS Analysis ID: 0713E2024 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
I. Equipo Médico
Product Type (English)
I. Equipo Médico
Trade Name (Spanish)
TOMÓGRAFO DE COHERENCIA ÓPTICA, MARCA: NIDEK, MODELO: RETINA SCAN DUO 2
Trade Name (English)
TOMÓGRAFO DE COHERENCIA ÓPTICA, MARCA: NIDEK, MODELO: RETINA SCAN DUO 2
Registration Information
Analysis ID
0713E2024 SSA
Registration Date
March 13, 2024
Manufacturer / Fabricante
Name (Spanish)
S4OPTIK, S.A. DE C.V.
Name (English)
S4OPTIK, S.A. DE C.V.