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DENGUE - ANVISA Registration 80524900079

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 80524900079 and manufactured by manufacturer not specified. The registration is held by BIO ADVANCE DIAGNOSTICOS LTDA with validity until Feb 22, 2031.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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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80524900079
2 Related Devices
Registration Details
ANVISA Registration Number: 80524900079
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Related Devices (2)

Teste Rรกpido OnSite Dengue IgG
Risk Class III

Registration Details

80524900079

25351924758202038

09593438000103

Company Information

Dates and Status

Feb 22, 2021

22/02/2031

09/18/2025 19:00:01

Teste Rรกpido OnSite Dengue IgG
Risk Class III

Registration Details

80524900079

25351924758202038

09593438000103

Company Information

CTK BIOTECH, INC.
United States of America
PT: ESTADOS UNIDOS DA AMร‰RICA

Dates and Status

Feb 22, 2021

22/02/2031

09/18/2025 19:00:01