DUS R-300 - COFEPRIS Registration 1056E2019 SSA
Access comprehensive regulatory information for DUS R-300 (DUS R-300) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1056E2019 SSA and manufactured by KANA UNDESA, S.A. DE C.V.. The device was registered on May 17, 2019.
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.
EL ANALIZADOR ES UN FOTÓMETRO DE REFLECTANCIA DESTINADO PARA MEDIR ALGUNAS DE LAS PROPIEDADES FÍSICAS Y COMPONENTES QUÍMICOS DE ORINA.
THE ANALYZER IS A REFLECTANCE PHOTOMETER INTENDED TO MEASURE SOME OF THE PHYSICAL PROPERTIES AND CHEMICAL COMPONENTS OF URINE.