AVITENE - COFEPRIS Registration 2059C2019 SSA
Access comprehensive regulatory information for AVITENE (AVITENE) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 2059C2019 SSA and manufactured by BECTON DICKINSON DE MÉXICO, S.A. DE C.V.. The device was registered on October 30, 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.
AVITENE (MCH) Y LA ESPONJA AVITENE ULTRAFOAM SE UTILIZAN EN PROCEDIMIENTOS QUIRÚRGICOS COMO RECURSO ADJUNTO A LA HEMOSTASIA CUANDO EL CONTROL DE LA HEMORRAGIA MEDIANTE PROCEDIMIENTOS CONVENCIONALES O LIGADURA ES INEFICAZ O NO ES PRÁCTICO.
AVITENE (MCH) AND AVITENE ULTRAFOAM SPONGE ARE USED IN SURGICAL PROCEDURES AS AN ADJUNCT RESOURCE TO HEMOSTASIS WHEN BLEEDING CONTROL BY CONVENTIONAL PROCEDURES OR LIGATION IS INEFFECTIVE OR IMPRACTICAL.