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

CORONAVIRUS - ANVISA Registration 80535240058

Access comprehensive regulatory information for CORONAVIRUS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80535240058 and manufactured by CHEMBIO DIAGNOSTICS BRAZIL LTDA.. The registration is held by CHEMBIO DIAGNOSTICS BRAZIL LTDA. with validity until Feb 08, 2031.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including GUANGZHOU WONDFO BIOTECH CO., LTD., Eco Diagnostica Ltda, 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
80535240058
2 Related Devices
Registration Details
ANVISA Registration Number: 80535240058
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Related Devices (2)

DPP® SARS CoV-2 IgM/IgG
Risk Class III

Registration Details

80535240058

25351626518202071

09449181000102

Company Information

Brazil
PT: BRASIL

Dates and Status

Feb 08, 2021

08/02/2031

09/18/2025 19:00:01

DPP® SARS CoV-2 IgM/IgG
Risk Class III

Registration Details

80535240058

25351626518202071

09449181000102

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Feb 08, 2021

08/02/2031

09/18/2025 19:00:01