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 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
10298910183
25351387280202486
00351210000124
Company Information
Dates and Status
Sep 16, 2024
VIGENTE
09/18/2025 19:00:01
Instrument for sample preparation and processing – pre-analytical phase
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Instrument for sample preparation and processing – pre-analytical phase
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Mar 07, 2016
Instrument for sample preparation and processing – pre-analytical phase
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Jul 07, 2025
Instrument for sample preparation and processing – pre-analytical phase
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80929400010
Sep 05, 2019
Instrument for sample preparation and processing – pre-analytical phase
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Apr 15, 2019
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Instrumento para preparo e processamento de amostras – fase pré-analítica
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