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 80115310290

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 80115310290 and manufactured by KOVALENT DO BRASIL LTDA. The registration is held by KOVALENT DO BRASIL LTDA with validity until May 15, 2033.

This page provides complete technical specifications for this device, 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
80115310290
Registration Details
ANVISA Registration Number: 80115310290
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

K-teste Dengue NS1
Risk Class III

Registration Details

80115310290

25351140365202231

04842199000156

Company Information

Brazil
PT: BRASIL

Dates and Status

May 15, 2023

15/05/2033

09/18/2025 19:00:01