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IN SITU HYBRIDIZATION - COMPLEMENTARY REAGENTS - ANVISA Registration 10358940097

Access comprehensive regulatory information for IN SITU HYBRIDIZATION - COMPLEMENTARY REAGENTS in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10358940097 and manufactured by LIFE TECHNOLOGIES HOLDINGS PTE LTD. The registration is held by LIFE TECHNOLOGIES BRASIL COMERCIO E INDUSTRIA DE PRODUTOS PARA BIOTECNOLOGIA LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 4 companies making the same product including AGILENT TECHNOLOGIES SINGAPORE (INTERNATIONAL) PTE LTD., ABBOTT MOLECULAR, 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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10358940097
Registration Details
ANVISA Registration Number: 10358940097
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Device Details

Família BigDye® Terminator Sequencing Standard
Risk Class I

Registration Details

10358940097

25351196602201831

63067904000154

Company Information

Singapore
PT: CINGAPURA, REPÚBLICA DA

Dates and Status

Aug 13, 2018

VIGENTE

09/18/2025 19:00:01