DENGUE - ANVISA Registration 10071770940

Access comprehensive regulatory information for DENGUE in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10071770940 and manufactured by ABBOTT DIAGNOSTICS KOREA INC.. The registration is held by ABBOTT DIAGNOSTICOS RAPIDOS S.A. with validity until Mar 25, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including Eco Diagnostica Ltda, HANGZHOU ALLTEST BIOTECH CO. 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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10071770940
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Registration Details
ANVISA Registration Number: 10071770940
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

BIOLINE Dengue IgG/IgM WB
Risk Class III

Registration Details

10071770940

25351298164202311

50248780000161

Company Information

South Korea
PT: CORÉIA DO SUL

Dates and Status

Mar 25, 2024

25/03/2034

09/18/2025 19:00:01

BIOLINE Dengue IgG/IgM WB
Risk Class III

Registration Details

10071770940

25351298164202311

50248780000161

Company Information

Dates and Status

Mar 25, 2024

25/03/2034

09/18/2025 19:00:01