KIT DE EXTRACCIÓN Y/O REPOSICIONAMIENTO DEL FILTRO DE VENA CAVA ALN
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.
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.
- 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.
- Analysis ID
- 1118C2019 SSA
- Registration Date
- May 22, 2019
- Name (Spanish)
- LEVBETH MEDICAL S.A. DE C.V.
- Name (English)
- LEVBETH MEDICAL S.A. DE C.V.
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.