APTUS. - COFEPRIS Registration 1196E2019 SSA
Access comprehensive regulatory information for APTUS. (APTUS.) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1196E2019 SSA and manufactured by KANA UNDESA, S.A. DE C.V.. The device was registered on May 31, 2019.
This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), 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.
PARA LA DETERMINACIÓN CUANTITATIVA DE LA HEMOGLOBINA Y EL HEMATOCRITO EN SANGRE CAPILAR O VENOSA. SOLO PARA USO DE DIAGNÓSTICO IN VITRO. PARA USO EXCLUSIVO EN LABORATORIOS CLÍNICOS O DE GABINETE.
FOR THE QUANTITATIVE DETERMINATION OF HEMOGLOBIN AND HEMATOCRIT IN CAPILLARY OR VENOUS BLOOD. FOR IN VITRO DIAGNOSTIC USE ONLY. FOR USE IN CLINICAL OR CABINET LABORATORIES ONLY.