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CORONAVIRUS - ANVISA Registration 81991520001

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 81991520001 and manufactured by NANTONG EGENS BIOTECHNOLOGY CO.,LTD. The registration is held by RADAC IMPORTADORA E DISTRIBUIDORA LTDA with validity until Jun 25, 2030.

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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81991520001
2 Related Devices
Registration Details
ANVISA Registration Number: 81991520001
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Related Devices (2)

COVID-19 IgG/IgM Rapid Test Kit
Risk Class III

Registration Details

81991520001

25351440206202071

08900095000373

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jun 25, 2020

25/06/2030

09/18/2025 19:00:01

COVID-19 IgG/IgM Rapid Test Kit
Risk Class III

Registration Details

81991520001

25351440206202071

08900095000373

Company Information

Dates and Status

Jun 25, 2020

25/06/2030

09/18/2025 19:00:01