IN SITU HYBRIDIZATION - COMPLEMENTARY REAGENTS - ANVISA Registration 80146501778

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 80146501778 and manufactured by ABBOTT MOLECULAR. The registration is held by ABBOTT LABORATORIOS 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, 4 companies making the same product including AGILENT TECHNOLOGIES SINGAPORE (INTERNATIONAL) PTE LTD., LEICA BIOSYSTEMS NEWCASTLE LTD, 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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80146501778
Registration Details
ANVISA Registration Number: 80146501778
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Device Details

Vysis Paraffin Pretreatment IV & Post-Hybridization Wash Buffer Kit
Risk Class I

Registration Details

80146501778

25351082557201298

56998701000116

Company Information

ABBOTT MOLECULAR
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Apr 02, 2012

VIGENTE

09/18/2025 19:00:01