FACTOR XII DEFICIENT PLASMA - COFEPRIS Registration 2148R2019 SSA
Access comprehensive regulatory information for FACTOR XII DEFICIENT PLASMA (FACTOR XII DEFICIENT PLASMA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2148R2019 SSA and manufactured by REPRESENTACIONES LABIN MÉXICO, S.A. DE C.V.. The device was registered on November 15, 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.
REACTIVO PARA LA DETERMINACIÓN COAGULOMÉTRICA EN UNA ETAPA DEL FACTOR XII. PARA USO DE DIAGNÓSTICO IN VITRO. AGENTE DE DIAGNÓSTICO PARA USO EXCLUSIVO DE LABORATORIO CLÍNICO O DE GABINETE
REAGENT FOR COAGULOMETRIC DETERMINATION IN ONE STEP OF FACTOR XII. FOR IN VITRO DIAGNOSTIC USE. DIAGNOSTIC AGENT FOR CLINICAL LABORATORY OR CABINET USE ONLY