N LÁTEX IGA - COFEPRIS Registration 773R2019 SSA
Access comprehensive regulatory information for N LÁTEX IGA (N LATEX IGA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 773R2019 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.. The device was registered on April 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.
REACTIVOS DE DIAGNÓSTICO IN-VITRO PARA LA DETERMINACIÓN CUANTITATIVA DE IGA EN LÍQUIDO CEFALORRAQUÍDEO (LCR) HUMANO Y EN MUESTRAS PAREADAS DE LCR Y SUERO POR MEDIO DE INMUNONEFELOMETRÍA CON PARTÍCULAS LÁTEX. AGENTE DE DIAGNÓSTICO. PARA USO EXCLUSIVO EN L
IN-VITRO DIAGNOSTIC REAGENTS FOR THE QUANTITATIVE DETERMINATION OF IGA IN HUMAN CEREBROSPINAL FLUID (CSF) AND PAIRED CSF AND SERUM SAMPLES BY MEANS OF LATEX PARTICLE IMMUNONEPHELOMETRY. DIAGNOSTIC AGENT. FOR USE IN L ONLY