QUANTA FLASH® CALPROTECTIN CALIBRATORS - COFEPRIS Registration 1075R2019 SSA
Access comprehensive regulatory information for QUANTA FLASH® CALPROTECTIN CALIBRATORS (QUANTA FLASH® CALPROTECTIN 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 1075R2019 SSA and manufactured by I.L. DIAGNOSTICS, S.A. DE C.V.. The device was registered on May 20, 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 CALPROTECTIN CALIBRATORS ESTÁN DESTINADOS A UTILIZARSE CON LOS REACTIVOS QUANTA FLASH CALPROTECTIN REAGENTS PARA LA DETERMINACIÓN DE LOS NIVELES DE CALPROTECTINA FECAL EN MUESTRAS DE HECES EXTRAÍDAS. CADA CALIBRADOR ESTABLECE UN PUNTO DE
QUANTA FLASH CALPROTECTIN CALIBRATORS ARE INTENDED FOR USE WITH QUANTA FLASH CALPROTECTIN REAGENTS FOR THE DETERMINATION OF FAECAL CALPROTECTIN LEVELS IN COLLECTED STOOL SAMPLES. EACH CALIBRATOR SETS A POINT OF