PAXGENE® BLOOD DNA TUBE - COFEPRIS Registration 2595R2018 SSA
Access comprehensive regulatory information for PAXGENE® BLOOD DNA TUBE (PAXGENE® BLOOD DNA TUBE) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2595R2018 SSA and manufactured by BECTON DICKINSON DE MÉXICO, S.A. DE C.V.. The device was registered on November 09, 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 TUBO DE ADN SANGUÍNEO PAXGENE ESTÁ DISEÑADO PARA LA EXTRACCIÓN, ANTICOAGULACIÓN, ESTABILIZACIÓN, TRANSPORTE Y CONSERVACIÓN DE UNA MUESTRA DE SANGRE ENTERA VENOSA PARA LA PREPARACIÓN DE ADN DE GRAN CALIDAD Y POSTERIOR USO EN PRUEBAS DIAGNÓSTICAS MOLECUL
THE PAXGENE BLOOD DNA TUBE IS DESIGNED FOR THE EXTRACTION, ANTICOAGULATION, STABILIZATION, TRANSPORT AND PRESERVATION OF A VENOUS WHOLE BLOOD SAMPLE FOR THE PREPARATION OF HIGH QUALITY DNA AND SUBSEQUENT USE IN MOLECULAR DIAGNOSTIC TESTS.