Instrument for sample preparation and processing – pre-analytical phase - ANVISA Registration 10287411141
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 10287411141 and manufactured by VENTANA MEDICAL SYSTEMS, INC. The registration is held by ROCHE DIAGNÓSTICA BRASIL 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.

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Registration Details
10287411141
25351831594201635
30280358000186
Company Information
Dates and Status
Jul 04, 2016
VIGENTE
09/18/2025 19:00:01
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