DENGUE - ANVISA Registration 10330660269

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 10330660269 and manufactured by manufacturer not specified. The registration is held by DESCARPACK DESCARTAVEIS DO BRASIL LTDA with validity until Sep 02, 2029.

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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10330660269
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Registration Details
ANVISA Registration Number: 10330660269
Janaina dos Santos de Miranda

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Related Devices (2)

TESTE RÁPIDO STANDARD Q DENGUE IgM/IgG
Risk Class III

Registration Details

10330660269

25351632021201877

01057428000133

Company Information

Dates and Status

Sep 02, 2019

02/09/2029

09/18/2025 19:00:01

TESTE RÁPIDO STANDARD Q DENGUE IgM/IgG
Risk Class III

Registration Details

10330660269

25351632021201877

01057428000133

Company Information

SD BIOSENSOR, INC.
South Korea
PT: CORÉIA DO SUL

Dates and Status

Sep 02, 2019

02/09/2029

09/18/2025 19:00:01