DENGUE - ANVISA Registration 82202950024

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 82202950024 and manufactured by manufacturer not specified. The registration is held by MICO BIOMED DO BRASIL LTDA with validity until Oct 02, 2033.

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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82202950024
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Registration Details
ANVISA Registration Number: 82202950024
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Kit Veri-Q pan-Dengue virus Detection
Risk Class III

Registration Details

82202950024

25351200795202481

40749573000137

Company Information

Dates and Status

Apr 29, 2024

02/10/2033

09/18/2025 19:00:01

Kit Veri-Q pan-Dengue virus Detection
Risk Class III

Registration Details

82202950024

25351200795202481

40749573000137

Company Information

South Korea
PT: CORÉIA DO SUL

Dates and Status

Apr 29, 2024

02/10/2033

09/18/2025 19:00:01