HUBI LH - COFEPRIS Registration 2183R2021 SSA
Access comprehensive regulatory information for HUBI LH (HUBI LH) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2183R2021 SSA and manufactured by KABLACOMERCIAL,S.A.DE C.V.. The device was registered on December 16, 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.
HUBILHESUNAPRUEBADEDIAGNÓSTICOINVITROBASADAENINMUNOCROMATOGRAFÍA.LA PRUEBA REQUIERE ANALIZARSE EN ELEQUIPO HUBI QUAN PRO, EL CUAL ES UNANALIZADOR DISEÑADO PARA LADETERMINACIÓN CUANTITATIVA DE LAHORMONALUTEINIZANTE(LH)ENMUESTRASHUMANAS DE SANGRE. AGENTE DEDIAGNÓSTICOPARAUSOINVITRO. PARAUSOEXCLUSIVO EN LABORATORIOS CLÍNICOS ODE GABINETE.
HUBILHESA invitrobasa diagnostic test in immunochromatography. THE TEST NEEDS TO BE ANALYZED IN THE HUBI QUAN PRO EQUIPMENT, WHICH IS AN ANALYZER DESIGNED FOR THE QUANTITATIVE DETERMINATION OF THE HORMONAL UTEINIZANTE(LH) IN HUMAN BLOOD SAMPLES. DIAGNOSTIC AGENTFORUSEINVITRO. FOR EXCLUSIVE USE IN CLINICAL LABORATORIES OR CABINET.