UREA. - COFEPRIS Registration 762R2021 SSA
Access comprehensive regulatory information for UREA. (UREA.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 762R2021 SSA and manufactured by HRD HIGHRESOLUTION DIAGNOSTICS, S.A. DEC.V.. The device was registered on April 29, 2021.
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 DE DIAGNÓSTICO PARA LADETERMINACIÓNCUANTITATIVAINVITRODEUREAENORINA,SUEROYPLASMAHUMANO.AGENTE DE DIAGNÓSTICO PARA USO INVITRO. PARA USO EXCLUSIVO ENLABORATORIOS CLÍNICOS O DE GABINETE.
DIAGNOSTIC REACTIVE FOR LADETERMINACIÓNCUANTITATIVAINVITRODEUREAENORINA,SUEROYPLASMAHUMANO. DIAGNOSTIC AGENT FOR INVITRO USE. FOR EXCLUSIVE USE CLINICAL LABORATORIES OR CABINET.