DENGUE - ANVISA Registration 10071770830

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 10071770830 and manufactured by ABBOTT DIAGNOSTICS KOREA INC.. The registration is held by ABBOTT DIAGNOSTICOS RAPIDOS S.A. with validity until May 31, 2026.

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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10071770830
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Registration Details
ANVISA Registration Number: 10071770830
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Dengue Early ELISA
Risk Class III

Registration Details

10071770830

25351788900201442

50248780000161

Company Information

South Korea
PT: CORÉIA DO SUL

Dates and Status

Mar 30, 2015

31/05/2026

09/18/2025 19:00:01

Dengue Early ELISA
Risk Class III

Registration Details

10071770830

25351788900201442

50248780000161

Company Information

Dates and Status

Mar 30, 2015

31/05/2026

09/18/2025 19:00:01