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TRUSELECT™. - COFEPRIS Registration 2170C2021 SSA

Access comprehensive regulatory information for TRUSELECT™. (TRUSELECT™.) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 2170C2021 SSA and manufactured by BOSTONSCIENTIFICDEMÉXICO, S.A. DE C.V.. The device was registered on December 15, 2021.

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
2170C2021 SSA
TRUSELECT™.
COFEPRIS Analysis ID: 2170C2021 SSA
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Product Use / Uso del Producto
Spanish

LOS MICROCATÉTERES TRUSELECT ESTÁNINDICADOS PARA USO VASCULARPERIFÉRICO. EL MICROCATÉTER SE PUEDEUTILIZAR PARA LA INFUSIÓN SELECTIVA DEMATERIALESDEDIAGNÓSTICO,EMBÓLICOSOTERAPÉUTICOS EN LOS VASOS.

English

TRUSELECT MICROCATHETERS ARE INDICATED FOR PERIPHERAL VASCULAR-PERIPHERAL USE. THE MICROCATHETER CAN BE USED FOR SELECTIVE INFUSION OF DIAGNOSTIC, EMBOLIC THERAPEUTIC MATERIALS INTO VESSELS.

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)
MICROCATÉTER.
Trade Name (English)
MICROCATÉTER.
Registration Information
Analysis ID
2170C2021 SSA
Registration Date
December 15, 2021
Manufacturer / Fabricante
Name (English)
BOSTONSCIENTIFICDEMÉXICO, S.A. DE C.V.