BK POLYOMAVIRUS - ANVISA Registration 81752180007

Access comprehensive regulatory information for BK POLYOMAVIRUS in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81752180007 and manufactured by ALTONA DIAGNOSTICS GMBH. The registration is held by ALTONA DIAGNOSTICS BRASIL 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 DIASORIN MOLECULAR LLC, ABBOTT MOLECULAR 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.