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KIT DE CATÉTER INTRATECAL ASCENDA - COFEPRIS Registration 951C2019 SSA

Access comprehensive regulatory information for KIT DE CATÉTER INTRATECAL ASCENDA (ASCEND INTRATHECAL CATHETER KIT) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 951C2019 SSA and manufactured by MEDTRONIC, S. DE R.L. DE C.V.. The device was registered on May 09, 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
951C2019 SSA
KIT DE CATÉTER INTRATECAL ASCENDA
COFEPRIS Analysis ID: 951C2019 SSA
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Product Use / Uso del Producto
Spanish

EL KIT DE CATÉTER INTRATECAL IMPLANTABLE ASCENDA FORMA PARTE DE UN SISTEMA DE INFUSIÓN QUE ALMACENA Y ADMINISTRA FÁRMACOS PARENTERALES EN EL ESPACIO INTRATECAL.

English

THE ASCENDA IMPLANTABLE INTRATHECAL CATHETER KIT IS PART OF AN INFUSION SYSTEM THAT STORES AND DELIVERS PARENTERAL DRUGS INTO THE INTRATHECAL SPACE.

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)
CATÉTER INTRATECAL
Trade Name (English)
INTRATHECAL CATHETER
Registration Information
Analysis ID
951C2019 SSA
Registration Date
May 09, 2019
Manufacturer / Fabricante
Name (English)
MEDTRONIC, S. DE R.L. DE C.V.