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CORONAVIRUS - ANVISA Registration 81991520005

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 81991520005 and manufactured by manufacturer not specified. The registration is held by RADAC IMPORTADORA E DISTRIBUIDORA LTDA with validity until Apr 12, 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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81991520005
2 Related Devices
Registration Details
ANVISA Registration Number: 81991520005
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Related Devices (2)

AllCheck COVID-19 IgG/IgM
Risk Class III

Registration Details

81991520005

25351958238202029

08900095000373

Company Information

Dates and Status

Apr 12, 2021

12/04/2031

09/18/2025 19:00:01

AllCheck COVID-19 IgG/IgM
Risk Class III

Registration Details

81991520005

25351958238202029

08900095000373

Company Information

CALTH INC.
South Korea
PT: CORÉIA DO SUL

Dates and Status

Apr 12, 2021

12/04/2031

09/18/2025 19:00:01