ROSE BENGAL KIT - COFEPRIS Registration 2295R2018 SSA
Access comprehensive regulatory information for ROSE BENGAL KIT (ROSE BENGAL KIT) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2295R2018 SSA and manufactured by KABLA COMERCIAL, S.A. DE C.V.. The device was registered on October 02, 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.
ES UNA PRUEBA DE AGLUTINACIÓN EN PORTAOBJETOS PARA LA DETECCIÓN CUALITATIVA Y SEMICUANTITATIVA DE ANTICUERPOS ANTI-BRUCELLA EN SUERO HUMANO
IT IS A SLIDE AGGLUTINATION TEST FOR THE QUALITATIVE AND SEMI-QUANTITATIVE DETECTION OF ANTI-BRUCELLA ANTIBODIES IN HUMAN SERUM