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CORONAVIRUS - ANVISA Registration 80430080010

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 80430080010 and manufactured by KH MEDICAL CO.LTD.. The registration is held by CMW SAUDE E TECNOLOGIA IMPORTAÇAO E EXPORTAÇAO LTDA - ME with validity until Feb 22, 2031.

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.

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80430080010
2 Related Devices
Registration Details
ANVISA Registration Number: 80430080010
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Related Devices (2)

TESTE RÁPIDO RADI COVID-19 Ag
Risk Class III

Registration Details

80430080010

25351900158202165

07430231000184

Company Information

KH MEDICAL CO.LTD.
South Korea
PT: CORÉIA DO SUL

Dates and Status

Feb 22, 2021

22/02/2031

09/18/2025 19:00:01

TESTE RÁPIDO RADI COVID-19 Ag
Risk Class III

Registration Details

80430080010

25351900158202165

07430231000184

Dates and Status

Feb 22, 2021

22/02/2031

09/18/2025 19:00:01