SET DE REACTIVOS PARACREATINA QUINASA LÍQUIDA. - COFEPRIS Registration 423R2022 SSA
Access comprehensive regulatory information for SET DE REACTIVOS PARACREATINA QUINASA LÍQUIDA. (SET OF LIQUID PARACREATINE KINASE REAGENTS.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 423R2022 SSA and manufactured by DICIPA, S.A. DE C.V.. The device was registered on May 25, 2022.
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.
SETDEREACTIVOSPARALADETERMINACIÓNCUANTITATIVADELAACTIVIDADDECREATININAQUINASAPRESENTEENELSUERO. AGENTEDEDIAGNÓSTICOPARAUSOINVITRO.PARAUSOEXCLUSIVODELABORATORIOSCLÍNICOSODEGABINETE.
SET of reagents for the quantitative determination of the activity of creatinine kinase present in serum. DIAGNOSTIC AGENTFOR use. FOR exclusive use of clinical laboratories or cabinets.