FLUID PACK 0018165300 - COFEPRIS Registration 1487R2020 SSA
Access comprehensive regulatory information for FLUID PACK 0018165300 (FLUID PACK 0018165300) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1487R2020 SSA and manufactured by I.L. DIAGNOSTICS, S.A. DE C.V.. The device was registered on October 29, 2020.
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.
FLUIDPACKSEUTILIZAPARALACALIBRACIรNDE SODIO, POTASIO Y CLORURO UTILIZANDOLOS ANALIZADORES DE QUรMICA CLรNICA ILAB.
FLUIDPACK IS USED FOR SODIUM, POTASSIUM AND CHLORIDE CALIBRATION USING ILAB CLINICAL CHEMISTRY ANALYZERS.

