TRUCLEAR SYSTEM - COFEPRIS Registration 878E2018 SSA
Access comprehensive regulatory information for TRUCLEAR SYSTEM (TRUCLEAR SYSTEM) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 878E2018 SSA and manufactured by KENDALL DE MÉXICO, S.A. DE C.V.. The device was registered on April 03, 2018.
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.
EL SISTEMA DE EXTIRPACIÓN DE TEJIDOS DE HISTEROSCOPIA TRUCLEAR SYSTEM ESTÁ INDICADO PARA USO INTRAUTERINO PARA RESECAR Y EXTIRPAR HISTEROSCÓPICAMENTE TEJIDOS DEL TIPO: • MIOMAS SUBMUCOSOS • PÓPILOS ENDOMETRIALES • RESTO DE LA CONCEPCIÓN RETENIDOS
THE TRUCLEAR SYSTEM HYSTEROSCOPY TISSUE REMOVAL SYSTEM IS INDICATED FOR INTRAUTERINE USE TO RESECT AND HYSTEROSCOPICALLY REMOVE TISSUES OF THE TYPE: • SUBMUCOSAL FIBROIDS • ENDOMETRIAL POPILES • REST OF CONCEPTION RETAINED