DENGUE - ANVISA Registration 10350840485

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 10350840485 and manufactured by manufacturer not specified. The registration is held by BIOSYS LTDA with validity until Sep 01, 2035.

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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10350840485
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Registration Details
ANVISA Registration Number: 10350840485
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

SGTi-flex Dengue IgM/IgG
Risk Class III

Registration Details

10350840485

25351013260202552

02220795000179

Company Information

Dates and Status

Sep 01, 2025

01/09/2035

09/18/2025 19:00:01

SGTi-flex Dengue IgM/IgG
Risk Class III

Registration Details

10350840485

25351013260202552

02220795000179

Company Information

SUGENTECH INC
South Korea
PT: CORÉIA DO SUL

Dates and Status

Sep 01, 2025

01/09/2035

09/18/2025 19:00:01