Multimodality diagnostic X-ray system, mobile - ANVISA Registration 80071260442

Access comprehensive regulatory information for Multimodality diagnostic X-ray system, mobile in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80071260442 and manufactured by manufacturer not specified. The registration is held by GE HEALTHCARE DO BRASIL COMERCIO E SERVICOS PARA EQUIPAMENTOS MEDICO-HOSPITALARES LTDA with validity until Jul 31, 2033.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 4 companies making the same product including MEDPHOTON GMBH, SHIMADZU CORPORATION KYOTO, 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.