Instrument for sample preparation and processing – pre-analytical phase - ANVISA Registration 10337990012

Access comprehensive regulatory information for Instrument for sample preparation and processing – pre-analytical phase in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10337990012 and manufactured by LEICA BIOSYSTEMS MELBOURNE PTY LTD. The registration is held by LEICA DO BRASIL IMPORTAÇÃO E COMÉRCIO LTDA. with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including EPPENDORF SE, SHANDON DIAGNOSTICS LIMITED, 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.