VIPER PRIMETM SYSTEM IMPLANTS - COFEPRIS Registration 956C2019 SSA
Access comprehensive regulatory information for VIPER PRIMETM SYSTEM IMPLANTS (VIPER PRIMETM SYSTEM IMPLANTS) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 956C2019 SSA and manufactured by JOHNSON & JOHNSON DE MÉXICO, S.A. DE C.V.. The device was registered on May 09, 2019.
This page provides complete registration details including product type (II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS), 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.
LOS TORNILLOS FENESTRADOS VIPER PRIME ESTÁN CONCEBIDOS PARA SER UTILIZADOS CON EL CEMENTO ESPINAL DE ALTA VISCOSIDAD CONFIDENCE PARA LA INMOVILIZACIÓN Y ESTABILIZACIÓN DE SEGMENTOS VERTEBRALES EN EL TRATAMIENTO DE INESTABILIDADES O DEFORMIDADES AGUDAS O C
VIPER PRIME FENESTRATED SCREWS ARE DESIGNED TO BE USED WITH CONFIDENCE HIGH VISCOSITY SPINAL CEMENT FOR THE IMMOBILIZATION AND STABILIZATION OF VERTEBRAL SEGMENTS IN THE TREATMENT OF ACUTE INSTABILITIES OR DEFORMITIES OR