DENGUE - ANVISA Registration 10350840471

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 10350840471 and manufactured by manufacturer not specified. The registration is held by BIOSYS LTDA with validity until Feb 24, 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Similar Products
5 Competitors
10350840471
2 Related Devices
Registration Details
ANVISA Registration Number: 10350840471
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Related Devices (2)

Família ichroma™ Dengue NS1 Ag
Risk Class III

Registration Details

10350840471

25351888934202494

02220795000179

Company Information

Dates and Status

Feb 24, 2025

24/02/2035

09/18/2025 19:00:01

Família ichroma™ Dengue NS1 Ag
Risk Class III

Registration Details

10350840471

25351888934202494

02220795000179

Company Information

BODITECH MED INC.
South Korea
PT: CORÉIA DO SUL

Dates and Status

Feb 24, 2025

24/02/2035

09/18/2025 19:00:01