VICTUS VERAFITTM PATIENT INTERFACE KIT - COFEPRIS Registration 935E2019 SSA
Access comprehensive regulatory information for VICTUS VERAFITTM PATIENT INTERFACE KIT (VICTUS VERAFITTM PATIENT INTERFACE KIT) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 935E2019 SSA and manufactured by BAUSCH & LOMB MÉXICO, S.A. DE C.V.. The device was registered on May 08, 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.
VICTUS VERAFITTM PATIENT INTERFACE KIT DEBE UTILIZARSE EXCLUSIVAMENTE PARA TRATAMIENTOS DE CATARATAS, EN CÓRNEA Y TERAPÉUTICOS CON LA PLATAFORMA VICTUSTM. EL KIT DE INTERFACES PARA EL PACIENTE VICTUS VERAFITTM CONSISTE EN UNA INTERFAZ 125 PARA EL PACIENTE
VICTUS VERAFITTM PATIENT INTERFACE KIT SHOULD BE USED EXCLUSIVELY FOR CATARACT, CORNEAL AND THERAPEUTIC TREATMENTS WITH THE VICTUSTM PLATFORM. THE VICTUS VERAFITTM PATIENT INTERFACE KIT CONSISTS OF A 125 PATIENT INTERFACE