DENGUE - ANVISA Registration 10158120739

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 10158120739 and manufactured by manufacturer not specified. The registration is held by BIOMERIEUX BRASIL INDUSTRIA E COMERCIO DE PRODUTOS LABORATORIAIS LTDA with validity until Dec 20, 2031.

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
10158120739
2 Related Devices
Registration Details
ANVISA Registration Number: 10158120739
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)

VIDAS ANTI-DENGUE IgM (DENM)
Risk Class III

Registration Details

10158120739

25351552913202191

33040635000171

Dates and Status

Dec 20, 2021

20/12/2031

09/18/2025 19:00:01

VIDAS ANTI-DENGUE IgM (DENM)
Risk Class III

Registration Details

10158120739

25351552913202191

33040635000171

Company Information

BIOMERIEUX SA
France
PT: FRANÇA

Dates and Status

Dec 20, 2021

20/12/2031

09/18/2025 19:00:01