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CORONAVIRUS - ANVISA Registration 80882270006

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 80882270006 and manufactured by manufacturer not specified. The registration is held by PARTS IMPORT COMÉRCIO DE IMPORTAÇÃO E EXPORTAÇÃO LTDA. with validity until Mar 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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80882270006
2 Related Devices
Registration Details
ANVISA Registration Number: 80882270006
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Related Devices (2)

COVID-19 Saliva Ag Test
Risk Class III

Registration Details

80882270006

25351046052202114

02322453000160

Dates and Status

Mar 22, 2021

22/03/2031

09/18/2025 19:00:01

COVID-19 Saliva Ag Test
Risk Class III

Registration Details

80882270006

25351046052202114

02322453000160

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Mar 22, 2021

22/03/2031

09/18/2025 19:00:01