SOLANA INSTRUMENT - COFEPRIS Registration 51E2020 SSA
Access comprehensive regulatory information for SOLANA INSTRUMENT (SOLANA INSTRUMENT) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 51E2020 SSA and manufactured by KABLA COMERCIAL, S.A. DEC.V.. The device was registered on January 16, 2020.
This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), 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.
ANALIZADOR CLÍNICO AUTONOMO UTILIZADOEN LABORATORIOS CLÍNICOS PARA DETECIÓNMOLECULAR QUE COMBINA UNAAMPLIFICACIÓN DEPENDIENTE-HELICASA CONLA DETECCIÓN DE FLUORESCENTE PARAPROCESA HASTA 12 TUBOS DE ANÁLISIS DEDIAGNÓSTICO.
SELF-CONTAINED CLINICAL ANALYZER USED IN CLINICAL LABORATORIES FOR MOLECULAR DETECTION THAT COMBINES HELICASE-DEPENDENT AMPLIFICATION WITH FLUORESCENT DETECTION TO PROCESS UP TO 12 DIAGNOSTIC ANALYSIS TUBES.