ALCATH - COFEPRIS Registration 1681C2021 SSA
Access comprehensive regulatory information for ALCATH (ALCATH) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1681C2021 SSA and manufactured by ASESORES MÉDICOBIOLÓGICOS, S.A. DEC.V.. The device was registered on October 22, 2021.
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.
TODOS LOS CATÉTERES DE LA FAMILIA DEPRODUCTOS ALCATH SON CATÉTERESTEMPORALES, DIRIGIBLESUNIDIRECCIONALMENTE Y TETRAPOLARESPARALAABLACIÓNINTRACARDIACAPORRFO PARA LA DETECCIÓN DE SEÑALESINTRACARDIACAS Y LA ESTIMULACIÓNDIAGNÓSTICA. ESTÁN DISEÑADOS PARA EL
ALL CATHETERS IN THE ALCATH PRODUCT FAMILY ARE TEMPORARY, UNIDIRECTIONALLY STEERABLE AND TETRAPOLAR CATHETERS FOR INTRACARDIAC ABLATIONPORRFO FOR INTRACARDIAC SIGNAL DETECTION AND DIAGNOSTIC STIMULATION. THEY ARE DESIGNED FOR THE