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SISTEMA DE STENT CORONARIO LIBERADOR DE SIROLIMUS SUPRAFLEX - COFEPRIS Registration 894C2018 SSA

Access comprehensive regulatory information for SISTEMA DE STENT CORONARIO LIBERADOR DE SIROLIMUS SUPRAFLEX (SIROLIMUS SUPRAFLEX ELUTING CORONARY STENT SYSTEM) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 894C2018 SSA and manufactured by LEVBETH MEDICAL, S.A. DE C.V.. The device was registered on April 05, 2018.

This page provides complete registration details including product type (II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS), 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
894C2018 SSA
SISTEMA DE STENT CORONARIO LIBERADOR DE SIROLIMUS SUPRAFLEX
COFEPRIS Analysis ID: 894C2018 SSA
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Product Use / Uso del Producto
Spanish

PARA MEJORAR EL DIรMETRO LUMINAL Y REDUCIR LA ESTENร“SIS PARA TRATAMIENTO DE LESIONES DE ARTERIA CORONARIA

English

TO IMPROVE LUMINAL DIAMETER AND REDUCE STRICTURE FOR TREATMENT OF CORONARY ARTERY LESIONS

Device Classification
Risk Class / Clase de Riesgo
Clase III
Product Type (Spanish)
II. PROTESIS, ร“RTESIS Y AYUDAS FUNCIONALES
Product Type (English)
II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS
Trade Name (Spanish)
SISTEMA DE STENT CORONARIO CON FรRMACO
Trade Name (English)
DRUG-BASED CORONARY STENT SYSTEM
Registration Information
Analysis ID
894C2018 SSA
Registration Date
April 05, 2018
Manufacturer / Fabricante
Name (English)
LEVBETH MEDICAL, S.A. DE C.V.