ARGYLE TM FISTULA CANNULA - COFEPRIS Registration 1625C2018 SSA
Access comprehensive regulatory information for ARGYLE TM FISTULA CANNULA (ARGYLE TM FISTULA CANNULA) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1625C2018 SSA and manufactured by KENDALL DE MÉXICO, S.A. DE C.V.. The device was registered on June 22, 2018.
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.
ARGYLE TM FISTULA CANNULA SE UTILIZA PARA OBTENER ACCESO VASCULAR PARA LA EXTRACCIÓN DE SANGRE Y LA RE-INFUSIÓN DE SANGRE DURANTE LA DIÁLISIS. LA CARACTERÍSTICA DE PREVENCIÓN DE PINCHAZOS CON LA AGUJA ESTÁ PROPUESTA PARA MINIMIZAR LAS HERIDAS ACCIDENTALES
ARGYLETM CANNULA FISTULA IS USED TO GAIN VASCULAR ACCESS FOR BLOOD COLLECTION AND BLOOD RE-INFUSION DURING DIALYSIS. NEEDLE STICK PREVENTION FEATURE IS PROPOSED TO MINIMIZE ACCIDENTAL INJURIES