HUBI PCT - COFEPRIS Registration 411R2019 SSA
Access comprehensive regulatory information for HUBI PCT (HUBI PCT) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 411R2019 SSA and manufactured by KABLA COMERCIAL, S.A. DE C.V.. The device was registered on February 28, 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.
HUBI PCT ES UNA PRUEBA PARA LA DETERMINACIÓN CUANTITATIVA DE PROCALCITONINA EN SUERO, PLASMA O SANGRE ENTERA HUMANA. DEBE USARSE CON EL EQUIPO HUBI-QUAN PRO.
HUBI PCT IS A TEST FOR THE QUANTITATIVE DETERMINATION OF PROCALCITONIN IN HUMAN SERUM, PLASMA OR WHOLE BLOOD. MUST BE USED WITH HUBI-QUAN PRO EQUIPMENT.