Instrument for sample preparation and processing – pre-analytical phase - ANVISA Registration 10298910183

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 10298910183 and manufactured by OMNI INTERNATIONAL, INC. The registration is held by REVVITY DO 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 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.