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 80423850001

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 80423850001 and manufactured by manufacturer not specified. The registration is held by W N COMÉRCIO IMPORTAÇÃO E REPRESENTAÇÕES LTDA with validity until May 21, 2030.

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
80423850001
2 Related Devices
Registration Details
ANVISA Registration Number: 80423850001
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Related Devices (2)

Asan Easy Test Covid-19 IgG_IgM
Risk Class III

Registration Details

80423850001

25351334916202063

03442420000116

Company Information

Dates and Status

May 21, 2020

21/05/2030

09/18/2025 19:00:01

Asan Easy Test Covid-19 IgG_IgM
Risk Class III

Registration Details

80423850001

25351334916202063

03442420000116

Company Information

South Korea
PT: CORÉIA DO SUL

Dates and Status

May 21, 2020

21/05/2030

09/18/2025 19:00:01