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Instrument for sample preparation and processing – pre-analytical phase - ANVISA Registration 81504790265

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 81504790265 and manufactured by HOLOGIC, INC.. The registration is held by PASSROD IMPORTAÇÃO E EXPORTAÇÃO DE PRODUTOS PARA SAÚDE LTDA - ME 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.

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81504790265
Registration Details
ANVISA Registration Number: 81504790265
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Device Details

Registration Details

81504790265

25351247825202170

26185222000110

Company Information

HOLOGIC, INC.
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Sep 09, 2021

VIGENTE

09/18/2025 19:00:01