Mexico COFEPRIS registration 1118C2019 SSA

KIT DE EXTRACCIÓN Y/O REPOSICIONAMIENTO DEL FILTRO DE VENA CAVA ALN

EN: ALN VENA CAVA FILTER EXTRACTION AND/OR REPOSITIONING KIT
Mexico flagMexico·Clase III·V. SURGICAL AND HEALING MATERIALS·LEVBETH MEDICAL S.A. DE C.V.·Registered May 22, 2019
Product Use / Uso del Producto
Spanish

EL KIT DE REPOSICIONAMIENTO Y/O EXTRACCIÓN DEL ALN FILTRO DE LA VENA CAVA HA SIDO DISEÑADO PARA LA EXTIRPACIÓN DE UN ALN FILTRO DE LA VENA CAVA O ALN FILTRO OPCIONAL DE LA VENA CAVA CON GANCHO IMPLANTADO EN PACIENTES QUE NO REQUIERAN MÁS UN FILTRO.

English

THE ALN VENA CAVA FILTER REPOSITIONING AND/OR REMOVAL KIT HAS BEEN DESIGNED FOR THE REMOVAL OF AN ALN VENA CAVA FILTER OR OPTIONAL ALN VENA CAVA FILTER WITH IMPLANTED HOOK IN PATIENTS WHO NO LONGER REQUIRE A FILTER.

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)
DISPOSITIVO PARA EXTRACCIÓN Y/O REPOSICIONAMIENTO DEL FILTRO DE VENA CAVA.
Trade Name (English)
DEVICE FOR EXTRACTION AND/OR REPOSITIONING OF THE VENA CAVA FILTER.
Registration information
Analysis ID
1118C2019 SSA
Registration Date
May 22, 2019
Manufacturer / Fabricante
Name (English)
LEVBETH MEDICAL S.A. DE C.V.
About this record

Access comprehensive regulatory information for KIT DE EXTRACCIÓN Y/O REPOSICIONAMIENTO DEL FILTRO DE VENA CAVA ALN (ALN VENA CAVA FILTER EXTRACTION AND/OR REPOSITIONING 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 1118C2019 SSA and manufactured by LEVBETH MEDICAL S.A. DE C.V.. The device was registered on May 22, 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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