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CORONAVIRUS - ANVISA Registration 81472060050

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 81472060050 and manufactured by manufacturer not specified. The registration is held by ADVAGEN BIOTECH LTDA with validity until Aug 25, 2035.

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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81472060050
2 Related Devices
Registration Details
ANVISA Registration Number: 81472060050
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Related Devices (2)

Teste Rápido COVID-19
Risk Class III

Registration Details

81472060050

25351070975202511

22565307000172

Company Information

Dates and Status

Aug 25, 2025

25/08/2035

09/18/2025 19:00:01

Teste Rápido COVID-19
Risk Class III

Registration Details

81472060050

25351070975202511

22565307000172

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Aug 25, 2025

25/08/2035

09/18/2025 19:00:01