CORONAVIRUS - ANVISA Registration 81914040002

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 81914040002 and manufactured by OSANG HEALTHCARE CO., LTD.. The registration is held by UNA MEDIC IMPORTAÇAO E EXPORTAÇAO LTDA with validity until May 21, 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
81914040002
2 Related Devices
Registration Details
ANVISA Registration Number: 81914040002
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)

GeneFinder COVID-19 Plus RealAmp Kit
Risk Class III

Registration Details

81914040002

25351363668202068

32247380000150

Company Information

South Korea
PT: CORÉIA DO SUL

Dates and Status

May 21, 2020

21/05/2030

09/18/2025 19:00:01

GeneFinder COVID-19 Plus RealAmp Kit
Risk Class III

Registration Details

81914040002

25351363668202068

32247380000150

Company Information

Dates and Status

May 21, 2020

21/05/2030

09/18/2025 19:00:01