ÁCIDO ÚRICO ERBA.
Mexico·Clase I·III. DIAGNOSTIC AGENTS·HRD HIGHRESOLUTION DIAGNOSTICS, S.A. DEC.V.·Registered April 26, 2021REACTIVO DE DIAGNÓSTICO PARA LADETERMINACIÓNCUANTITATIVAINVITRODEÁCIDO ÚRICO EN ORINA, SUERO Y PLASMAHUMANO. AGENTESDEDIAGNÓSTICOPARAUSO IN VITRO, PARA USO EXCLUSIVO ENLABORATORIOS CLÍNICOS Ó DE GABINETE.
DIAGNOSTIC REAGENT FOR QUANTITATIVE DETERMINATIONINVITRODEURURIC ACID IN URINE, SERUM AND HUMAN PLASMA. DIAGNOSTIC AGENTS FOR IN VITRO USE, FOR EXCLUSIVE USE IN CLINICAL OR CABINET LABORATORIES.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- REACTIVOS PARA LA DETERMINACIÓNCUANTITATIVA DE ÁCIDO ÚRICO.
- Trade Name (English)
- REAGENTS FOR THE QUANTITATIVE DETERMINATION OF URIC ACID.
- Analysis ID
- 723R2021 SSA
- Registration Date
- April 26, 2021
- Name (Spanish)
- HRD HIGHRESOLUTION DIAGNOSTICS, S.A. DEC.V.
- Name (English)
- HRD HIGHRESOLUTION DIAGNOSTICS, S.A. DEC.V.
Access comprehensive regulatory information for ÁCIDO ÚRICO ERBA. (URIC ACID ERBA.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 723R2021 SSA and manufactured by HRD HIGHRESOLUTION DIAGNOSTICS, S.A. DEC.V.. The device was registered on April 26, 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.