CORONAVIRUS - ANVISA Registration 80560310070

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 80560310070 and manufactured by ACON BIOTECH (HANGZHOU)CO.,LTD.. The registration is held by MEDLEVENSOHN COMÉRCIO E REPRESENTAÇÕES DE PRODUTOS HOSPITALARES LTDA with validity until Apr 05, 2031.

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
80560310070
2 Related Devices
Registration Details
ANVISA Registration Number: 80560310070
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)

Teste Rápido Coronavírus (Covid-19) IgG/IgM
Risk Class III

Registration Details

80560310070

25351143709202182

05343029000190

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Apr 05, 2021

05/04/2031

09/18/2025 19:00:01

Teste Rápido Coronavírus (Covid-19) IgG/IgM
Risk Class III

Registration Details

80560310070

25351143709202182

05343029000190

Dates and Status

Apr 05, 2021

05/04/2031

09/18/2025 19:00:01