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CREATINAS. - COFEPRIS Registration 658R2021 SSA

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.

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COFEPRIS Official Data
Clase I
658R2021 SSA
CREATINAS.
COFEPRIS Analysis ID: 658R2021 SSA
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Product Use / Uso del Producto
Spanish

REACTIVO PARA LA DETERMINACIร“NCUANTITATIVA IN VITRO DE LA CREATINAQUINASA EN SUERO Y PLASMA HUMANOS.PARA USO EXCLUSIVO EN LABORATORIOCLรNICO Y DE GABINETE.

English

REAGENT FOR THE QUANTITATIVE DETERMINATION IN VITRO OF CREATINE KINASE IN HUMAN SERUM AND PLASMA. FOR EXCLUSIVE USE IN CLINICAL LABORATORY AND CABINET.

Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. AGENTES DE DIAGNร“STICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
REACTIVO PARA DIAGNร“STICO IN VITROPARA CREATINA.
Trade Name (English)
IN VITRO DIAGNOSTIC REAGENT FOR CREATINE.
Registration Information
Analysis ID
658R2021 SSA
Registration Date
April 16, 2021
Manufacturer / Fabricante
Name (English)
HRD HIGHRESOLUTION DIAGNOSTICS, S.A. DEC.V.