Mexico COFEPRIS registration 886C2019 SSA

HYBRID WIRE

EN: HYBRID WIRE
Mexico flagMexico·Clase III·V. SURGICAL AND HEALING MATERIALS·ISA HEALTH, S.A DE C.V.·Registered April 30, 2019
Product Use / Uso del Producto
Spanish

DISPOSITIVO QUE SE UTILIZA PARA FACILITAR LA COLOCACIÓN DE CATÉTERES PARA USO DIAGNÓSTICO O TERAPÉUTICO EN EL ÁRBOL VASCULAR INTRACRANEAL

English

DEVICE USED TO FACILITATE PLACEMENT OF CATHETERS FOR DIAGNOSTIC OR THERAPEUTIC USE IN THE INTRACRANIAL VASCULAR TREE

Device classification
Risk Class / Clase de Riesgo
Clase III
Product Type (Spanish)
V. MATERIALES QUIRÚRGICOS Y DE CURACIÓN
Product Type (English)
V. SURGICAL AND HEALING MATERIALS
Trade Name (Spanish)
GUÍA DE CATÉTER
Trade Name (English)
CATHETER GUIDE
Registration information
Analysis ID
886C2019 SSA
Registration Date
April 30, 2019
Manufacturer / Fabricante
Name (English)
ISA HEALTH, S.A DE C.V.
About this record

Access comprehensive regulatory information for HYBRID WIRE (HYBRID WIRE) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 886C2019 SSA and manufactured by ISA HEALTH, S.A DE C.V.. The device was registered on April 30, 2019.

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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