KIT HEVYLITE® IGG LAMBDA OPTILITE® - COFEPRIS Registration 268R2019 SSA
Access comprehensive regulatory information for KIT HEVYLITE® IGG LAMBDA OPTILITE® (KIT HEVYLITE® IGG LAMBDA OPTILITE®) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 268R2019 SSA and manufactured by INSUMOS PARA LA SALUD, S.A. DE C.V.. The device was registered on February 12, 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.
EL KIT HEVYLITE® IGG LAMBDA OPTILITE® ES UN ENSAYO IN VITRO CUANTITATIVO QUE PERMITE MEDIR LA IGG LAMBDA (CADENA PESADA IGG Y CADENA LIGERA LAMBDA DE INMUNOGLOBULINA INTACTA) EN SUERO O PLASMA OBTENIDA CON HEPARINA LITIO O EDTA, USANDO EL ANALIZADOR OPTIL
THE HEVYLITE® IGG LAMBDA OPTILITE® KIT IS A QUANTITATIVE IN VITRO ASSAY THAT ALLOWS MEASURING IGG LAMBDA (IGG HEAVY CHAIN AND INTACT IMMUNOGLOBULIN LAMBDA LIGHT CHAIN) IN SERUM OR PLASMA OBTAINED WITH LITHIUM HEPARIN OR EDTA, USING THE OPTIL ANALYZER