IGA-C - COFEPRIS Registration 1386R2020 SSA
Access comprehensive regulatory information for IGA-C (E-C) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1386R2020 SSA and manufactured by PRODUCTOS ROCHE, S.A. DEC.V.. The device was registered on October 12, 2020.
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.
PRUEBA IN VITRO PARA LA DETERMINACIรNCUANTITATIVA DE LA INMUNOGLOBULINA A(IGA)ENLรQUIDOCEFALORRAQUรDEOHUMANOY DE FORMA PARALELA EN SUERO/PLASMAHUMANO EN LOS SISTEMAS ROCHE
IN VITRO TEST FOR THE QUANTITATIVE DETERMINATION OF IMMUNOGLOBULIN A (IGA) IN CEREBROSPINAL FLUID OR HUMAN AND IN PARALLEL IN HUMAN SERUM / PLASMA IN ROCHE SYSTEMS

