FORESIGHT® HBSAG EIA TEST KIT (KIT DE PRUEBA HBSAG EIA) - COFEPRIS Registration 2673R2018 SSA
Access comprehensive regulatory information for FORESIGHT® HBSAG EIA TEST KIT (KIT DE PRUEBA HBSAG EIA) (FORESIGHT® HBSAG EIA TEST KIT (KIT DE PRUEBA HBSAG EIA)) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 2673R2018 SSA and manufactured by KABLA COMERCIAL, S.A. DE C.V.. The device was registered on November 29, 2018.
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.
FORESIGHT® HBSAG EIA TEST KIT (KIT DE PRUEBA HBSAG EIA), ES UNA PRUEBA PARA LA DETECCIÓN DE ANTICUERPOS DE HEPATITIS B EN SUERO O PLASMA HUMANO.
FORESIGHT® HBSAG EIA TEST KIT IS A TEST FOR THE DETECTION OF HEPATITIS B ANTIBODIES IN HUMAN SERUM OR PLASMA.

