DENGUE - ANVISA Registration 80524900032

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 80524900032 and manufactured by CTK BIOTECH, INC.. The registration is held by BIO ADVANCE DIAGNOSTICOS LTDA with validity until Dec 07, 2025.

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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80524900032
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Registration Details
ANVISA Registration Number: 80524900032
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Teste Rápido OnSite Dengue Ag
Risk Class III

Registration Details

80524900032

25351561111201539

09593438000103

Company Information

CTK BIOTECH, INC.
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Dec 07, 2015

07/12/2025

09/18/2025 19:00:01

Teste Rápido OnSite Dengue Ag
Risk Class III

Registration Details

80524900032

25351561111201539

09593438000103

Company Information

Dates and Status

Dec 07, 2015

07/12/2025

09/18/2025 19:00:01