Instrument for urine analysis - ANVISA Registration 80405180005

Access comprehensive regulatory information for Instrument for urine analysis in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80405180005 and manufactured by DFI CO., LTD. The registration is held by DIAGMAX REPRESENTAÇÃO E COMÉRCIO DE PRODUTOS MÉDICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including URIT MEDICAL ELECTRONIC CO LTD, BIOWAY BIOLOGICAL TECHNOLOGY CO. LTD, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.