KIT C1 INACTIVADOR OPTILITE® - COFEPRIS Registration 1919R2018 SSA
Access comprehensive regulatory information for KIT C1 INACTIVADOR OPTILITE® (KIT C1 INACTIVADOR 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 1919R2018 SSA and manufactured by INSUMOS PARA LA SALUD, S.A. DE C.V.. The device was registered on August 06, 2018.
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 C1 INACTIVADOR OPTILITE® TIENE COMO OBJETIVO LA CUANTIFICACIÓN IN VITRO DE C1 INACTIVADOR EN SUERO O EN PLASMA OBTENIDO CON HEPARINA LITIO O EDTA, EN EL ANALIZADOR OPTILITE® DE BINDING SITE, COMO AYUDA EN EL DIAGNÓSTICO DEL ANGIOEDEMA HEREDITARIO (
THE C1 OPTILITE INACTIVATOR KIT AIMS AT THE IN VITRO QUANTIFICATION OF C1 INACTIVATOR IN SERUM OR PLASMA OBTAINED WITH LITHIUM HEPARIN OR EDTA, IN THE BINDING SITE OPTILITE®® ANALYZER, AS AN AID IN THE DIAGNOSIS OF HEREDITARY ANGIOEDEMA (