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OPTICROSS 18 - COFEPRIS Registration 35C2020 SSA

Access comprehensive regulatory information for OPTICROSS 18 (OPTICROSS 18) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 35C2020 SSA and manufactured by BOSTON SCIENTIFIC DEMÉXICO, S.A. DE C.V.. The device was registered on January 10, 2020.

This page provides complete registration details including product type (V. SURGICAL AND HEALING MATERIALS), 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
35C2020 SSA
OPTICROSS 18
COFEPRIS Analysis ID: 35C2020 SSA
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Product Use / Uso del Producto
Spanish

EL CATÉTER OPTICROSS 18 ESTÁ DISEÑADOPARA SU UTILIZACIÓN EN ECOGRAFÍASINTRAVASCULARESDELOSVASOSPERIFÉRICOSÚNICAMENTE.

English

THE OPTICROSS 18 CATHETER IS DESIGNED FOR USE IN INTRAVASCULAR ULTRASOUND OF PERIPHERAL VESSELS ONLY.

Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
V. MATERIALES QUIRÚRGICOS Y DE CURACIÓN
Product Type (English)
V. SURGICAL AND HEALING MATERIALS
Trade Name (Spanish)
CATÉTER ECOGRÁFICO PERIFÉRICO
Trade Name (English)
PERIPHERAL ULTRASOUND CATHETER
Registration Information
Analysis ID
35C2020 SSA
Registration Date
January 10, 2020
Manufacturer / Fabricante
Name (English)
BOSTON SCIENTIFIC DEMÉXICO, S.A. DE C.V.