DIFF LYSE - COFEPRIS Registration 925R2018 SSA
Access comprehensive regulatory information for DIFF LYSE (DIFF LYSE) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 925R2018 SSA and manufactured by ATYDE MÉXICO, S.A. DE C.V.. The device was registered on April 10, 2018.
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.
ESTE PRODUCTO ES UTILIZADO PARA LISAR GLÓBULOS ROJOS Y MANTENER LA MORFOLOGÍA CELULAR NECESARIA PARA ANALIZAR LAS CÉLULAS SANGUÍNEAS. PARA USO EXCLUSIVO EN LABORATORIOS CLÍNICOS Y GABINETES
THIS PRODUCT IS USED TO LYSE RED BLOOD CELLS AND MAINTAIN THE CELLULAR MORPHOLOGY NEEDED TO ANALYZE BLOOD CELLS. FOR USE IN CLINICAL LABORATORIES AND CABINETS ONLY.