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CORONAVIRUS - ANVISA Registration 80262280031

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 80262280031 and manufactured by manufacturer not specified. The registration is held by ASSUT EUROPE LATINO AMERICA IMPORTAÇÃO E EXPORTAÇÃO LTDA with validity until Apr 26, 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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80262280031
2 Related Devices
Registration Details
ANVISA Registration Number: 80262280031
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Related Devices (2)

SARS-CoV-2 Antigen Rapid Swab
Risk Class III

Registration Details

80262280031

25351220804202115

07032636000164

Dates and Status

Apr 26, 2021

26/04/2031

09/18/2025 19:00:01

SARS-CoV-2 Antigen Rapid Swab
Risk Class III

Registration Details

80262280031

25351220804202115

07032636000164

Company Information

ASSUT EUROPE SPA
Italy
PT: ITÁLIA

Dates and Status

Apr 26, 2021

26/04/2031

09/18/2025 19:00:01