BIZACT™ TONSILLECTOMY DEVICE - COFEPRIS Registration 1631E2019 SSA
Access comprehensive regulatory information for BIZACT™ TONSILLECTOMY DEVICE (BIZACT™ TONSILLECTOMY DEVICE) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1631E2019 SSA and manufactured by KENDALL DE MÉXICO, S.A. DE C.V.. The device was registered on August 15, 2019.
This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), 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.
DISPOSITIVO INDICADO PARA SU USO EN PROCEDIMIENTOS GENERALES DE CIRUGÍA ABIERTA. DISEÑADO PARA SU USO EN PROCEDIMIENTOS DE CIRUGÍA ABIERTA EN LOS QUE SE DESEE LIGAR Y DIVIDIR VASOS, HACES DE TEJIDOS Y GANGLIOS LINFÁTICOS. LA FUNCIÓN DE FUSIÓN DE TEJIDOS
DEVICE INDICATED FOR USE IN GENERAL OPEN SURGERY PROCEDURES. DESIGNED FOR USE IN OPEN SURGERY PROCEDURES IN WHICH IT IS DESIRED TO LIGATE AND DIVIDE VESSELS, TISSUE BUNDLES AND LYMPH NODES. THE TISSUE FUSION FUNCTION