DIBU. - COFEPRIS Registration 1307R2021 SSA
Access comprehensive regulatory information for DIBU. (DIBU.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1307R2021 SSA and manufactured by PRODUCTOS ROCHE,S.A. DE C.V.. The device was registered on August 31, 2021.
This page provides complete registration details including product type (III. DIAGNOSTIC AGENTS), 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.
REACTIVOPARALADETERMINACIÓNINVITRODELNÚMERODEDIBUCAÍNAQUESEUTILIZAJUNTO CON EL TEST IN VITROCHOLINESTERASE GEN.2, EN LOS SISTEMASROCHE. AGENTES DE DIAGNÓSTICO PARAUSO IN VITRO, PARA USO EXCLUSIVO ENLABORATORIOS CLÍNICOS Ó DE GABINETE
REAGENT FOR THE DETERMINATION OF THE NUMBER OF DIBUCAINE, WHICH IS USED TOGETHER WITH THE IN VITROCHOLINESTERASE GEN.2 TEST, IN ROCHE SYSTEMS. DIAGNOSTIC AGENTS FOR IN VITRO USE, FOR EXCLUSIVE USE IN CLINICAL OR CABINET LABORATORIES