CREATINAS.
Mexico·Clase I·III. DIAGNOSTIC AGENTS·HRD HIGHRESOLUTION DIAGNOSTICS, S.A. DEC.V.·Registered April 16, 2021REACTIVO PARA LA DETERMINACIÓNCUANTITATIVA IN VITRO DE LA CREATINAQUINASA EN SUERO Y PLASMA HUMANOS.PARA USO EXCLUSIVO EN LABORATORIOCLÍNICO Y DE GABINETE.
REAGENT FOR THE QUANTITATIVE DETERMINATION IN VITRO OF CREATINE KINASE IN HUMAN SERUM AND PLASMA. FOR EXCLUSIVE USE IN CLINICAL LABORATORY AND CABINET.
- Risk Class / Clase de Riesgo
- Clase I
- Product Type (Spanish)
- III. AGENTES DE DIAGNÓSTICO
- Product Type (English)
- III. DIAGNOSTIC AGENTS
- Trade Name (Spanish)
- REACTIVO PARA DIAGNÓSTICO IN VITROPARA CREATINA.
- Trade Name (English)
- IN VITRO DIAGNOSTIC REAGENT FOR CREATINE.
- Analysis ID
- 658R2021 SSA
- Registration Date
- April 16, 2021
- Name (Spanish)
- HRD HIGHRESOLUTION DIAGNOSTICS, S.A. DEC.V.
- Name (English)
- HRD HIGHRESOLUTION DIAGNOSTICS, S.A. DEC.V.
Access comprehensive regulatory information for CREATINAS. (CHRYSEINES.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 658R2021 SSA and manufactured by HRD HIGHRESOLUTION DIAGNOSTICS, S.A. DEC.V.. The device was registered on April 16, 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.