HUBI TSH - COFEPRIS Registration 1341R2021 SSA
Access comprehensive regulatory information for HUBI TSH (HUBI TSH) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1341R2021 SSA and manufactured by KABLACOMERCIAL,S.A.DE C.V.. The device was registered on June 09, 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.
HUBITSHESUNAPRUEBADIAGNÓSTICAINVITRO DE UN SOLO PASO BASADA ENINMUNOCROMATOGRAFÍA. DEBE UTILIZARSECONHUBIQUANPROYESTÁDISEÑADAPARALA DETERMINACIÓN CUANTITATIVA DE LAHORMONA ESTIMULANTE DE LA TIROIDES(TSH, POR SUS SINGLAS EN INGLÉS) ENSUERO,PLASMAOSANGREHUMANAENTERA.AGENTEDEDIAGNÓSTICODEUSOINVITRO.PARA USO EXCLUSIVO DE LABORATORIOCLÍNICO O DE GABINETE.
HUBITSHESA ONE-STEP DIAGNOSTIC TEST BASED ON IMMUNOCHROMATOGRAPHY. IT SHOULD BE USED WITH HUBIQUAN PROAND IS DESIGNED FOR THE QUANTITATIVE DETERMINATION OF THYROID-STIMULATING HORMONE (TSH) IN SERUM, PLASMA OR WHOLE HUMAN BLOOD. DIAGNOSTICAGENT ofuseinvitro. FOR CLINICAL LABORATORY OR CABINET USE ONLY.