QUANTA FLASH® LKM-1 CALIBRATORS - COFEPRIS Registration 1003R2019 SSA
Access comprehensive regulatory information for QUANTA FLASH® LKM-1 CALIBRATORS (QUANTA FLASH® LKM-1 CALIBRATORS) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1003R2019 SSA and manufactured by I.L. DIAGNOSTICS, S.A. DE C.V.. The device was registered on May 15, 2019.
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.
LOS QUANTA FLASH LKM-1 CALIBRATORS SE UTILIZAN CON LOS QUANTA FLASH LKM-1 REAGENTS PARA LA DETERMINACIÓN DE AUTOANTICUERPOS IGG ANTI-LKM-1 EN SUERO HUMANO. AGENTE DE DIAGNÓSTICO PARA USO IN VITRO. PARA USO EXCLUSIVO DE LABORATORIOS CLÍNICOS O DE GABINE
QUANTA FLASH LKM-1 CALIBRATORS ARE USED WITH QUANTA FLASH LKM-1 REAGENTS FOR THE DETERMINATION OF ANTI-LKM-1 IGG AUTOANTIBODIES IN HUMAN SERUM. DIAGNOSTIC AGENT FOR IN VITRO USE. FOR USE BY CLINICAL LABORATORIES OR GABINE ONLY