XS LYSE - COFEPRIS Registration 1367R2019 SSA
Access comprehensive regulatory information for XS LYSE (XS BRIGHT) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1367R2019 SSA and manufactured by REPRESENTACIONES LABIN MÉXICO, S.A. DE C.V.. The device was registered on July 17, 2019.
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.
REACTIVO PARA LA DETERMINACIÓN CUANTITATIVA DE HEMOGLOBINA Y EL RECUENTO DE LEUCOCITOS. AGENTE DE DIAGNÓSTICO PARA USO IN VITRO. PARA USO EXCLUSIVO EN LABORATORIOS CLÍNICOS O DE GABINETES.
REAGENT FOR THE QUANTITATIVE DETERMINATION OF HEMOGLOBIN AND LEUKOCYTE COUNT. DIAGNOSTIC AGENT FOR IN VITRO USE. FOR USE IN CLINICAL OR CABINET LABORATORIES ONLY.