ENDOFAST VT GUIDE - COFEPRIS Registration 2019E2019 SSA
Access comprehensive regulatory information for ENDOFAST VT GUIDE (ENDOFAST VT GUIDE) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2019E2019 SSA and manufactured by LEVBETH MEDICAL, S.A. DE C.V.. The device was registered on October 21, 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.
LA ENDOFAST VT GUIDE HA SIDO DISEÑADA PARA RETRACCIÓN DURANTE PROCEDIMIENTOS QUIRÚRGICOS TRANSVAGINALES, COMO LA REPARACIÓN QUIRÚRGICA ANTERIOR Y POSTERIOR DEL PROLAPSO PÉLVICO DEL ÓRGANO.
THE ENDOFAST VT GUIDE HAS BEEN DESIGNED FOR RETRACTION DURING TRANSVAGINAL SURGICAL PROCEDURES, SUCH AS ANTERIOR AND POSTERIOR SURGICAL REPAIR OF PELVIC ORGAN PROLAPSE.