ALINITY C PREALBUMIN. - COFEPRIS Registration 2009R2021 SSA
Access comprehensive regulatory information for ALINITY C PREALBUMIN. (ALINITY C PREALBUMIN.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2009R2021 SSA and manufactured by ABBOTT LABORATORIES DEMÉXICO, S.A. DE C.V.. The device was registered on November 30, 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.
ELENSAYOPREALBUMINSEUTILIZAPARALADETERMINACIÓN CUANTITATIVA DEPREALBÚMINA EN SUERO HUMANO EN ELALINITY C SYSTEM. AGENTE DEDIAGNÓSTICOPARAUSOINVITRO. PARAUSOEXCLUSIVOENLABORATORIOSCLÍNICOSYDEGABINETE.
THE PREALBUMIN ASSAY IS USED FOR THE QUANTITATIVE DETERMINATION OF PREALBUMIN IN HUMAN SERUM IN ELALINITY C SYSTEM. DIAGNOSTIC AGENTFORUSEINVITRO. FOR exclusive use in clinical and cabinet laboratories.