CORONAVIRUS - ANVISA Registration 80772110001

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 80772110001 and manufactured by SHANGHAI OUTDO BIOTECH CO.,LTD.. The registration is held by YIN´S BRASIL COMERCIO INTERNACIONAL LTDA with validity until May 28, 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
80772110001
2 Related Devices
Registration Details
ANVISA Registration Number: 80772110001
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)

Test IgM/IgG SARS-CO-2
Risk Class III

Registration Details

80772110001

25351330664202001

02462686000168

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

May 28, 2020

28/05/2030

09/18/2025 19:00:01

Test IgM/IgG SARS-CO-2
Risk Class III

Registration Details

80772110001

25351330664202001

02462686000168

Company Information

Dates and Status

May 28, 2020

28/05/2030

09/18/2025 19:00:01