Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

DENGUE - ANVISA Registration 81987060018

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 81987060018 and manufactured by manufacturer not specified. The registration is held by BRAZIL IMPORT SOLUCOES PARA SAUDE LTDA with validity until Jun 30, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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 Competitors
5 Recent Registrations
81987060018
2 Related Devices
Registration Details
ANVISA Registration Number: 81987060018
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Related Devices (2)

QuickProfileโ„ข Dengue NS1 Antigen Test Card
Risk Class III

Registration Details

81987060018

25351426736202431

34625205000184

Company Information

Dates and Status

Jun 30, 2025

30/06/2035

09/18/2025 19:00:01

QuickProfileโ„ข Dengue NS1 Antigen Test Card
Risk Class III

Registration Details

81987060018

25351426736202431

34625205000184

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMร‰RICA

Dates and Status

Jun 30, 2025

30/06/2035

09/18/2025 19:00:01