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VASCO+ - COFEPRIS Registration 885C2019 SSA

Access comprehensive regulatory information for VASCO+ (BASQUE+) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 885C2019 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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COFEPRIS Official Data
Clase III
885C2019 SSA
VASCO+
COFEPRIS Analysis ID: 885C2019 SSA
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Product Use / Uso del Producto
Spanish

DISPOSITIVO QUE SE UTILIZA PARA LA INYECCIร“N DE PRODUCTOS DE DIAGNร“STICO O TERAPร‰UTICOS.

English

A DEVICE USED FOR THE INJECTION OF DIAGNOSTIC OR THERAPEUTIC PRODUCTS.

Device Classification
Risk Class / Clase de Riesgo
Clase III
Product Type (Spanish)
V. MATERIALES QUIRรšRGICOS Y DE CURACIร“N
Product Type (English)
V. SURGICAL AND HEALING MATERIALS
Trade Name (Spanish)
MICROCATร‰TER DE FLEXIBILIDAD PROGRESIVA
Trade Name (English)
PROGRESSIVE FLEXIBILITY MICROCATHETER
Registration Information
Analysis ID
885C2019 SSA
Registration Date
April 30, 2019
Manufacturer / Fabricante
Name (English)
ISA HEALTH, S.A DE C.V.