Multimodality diagnostic X-ray system, mobile - ANVISA Registration 80042070070

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 80042070070 and manufactured by MEDPHOTON GMBH. The registration is held by BRAINLAB LTDA with validity until Feb 22, 2033.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including SHIMADZU CORPORATION KYOTO, CARESTREAM HEALTH, INC, 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.