CORONAVIRUS - ANVISA Registration 80258020106

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 80258020106 and manufactured by manufacturer not specified. The registration is held by CEPALAB LABORATÓRIOS LTDA with validity until Apr 06, 2030.

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 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 Similar Products
5 Competitors
80258020106
2 Related Devices
Registration Details
ANVISA Registration Number: 80258020106
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)

COVID-19 IgG/IgM
Risk Class III

Registration Details

80258020106

25351219360202086

02248312000144

Company Information

Dates and Status

Apr 06, 2020

06/04/2030

09/18/2025 19:00:01

COVID-19 IgG/IgM
Risk Class III

Registration Details

80258020106

25351219360202086

02248312000144

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Apr 06, 2020

06/04/2030

09/18/2025 19:00:01