CORONAVIRUS - ANVISA Registration 80313210031

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 80313210031 and manufactured by manufacturer not specified. The registration is held by MP BIOMEDICALS DO BRASIL LTDA with validity until Mar 11, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 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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80313210031
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Registration Details
ANVISA Registration Number: 80313210031
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

RAPID SARS-CoV-2 ANTIGEN TEST CARD
Risk Class III

Registration Details

80313210031

25351758805202391

07776689000190

Company Information

Dates and Status

Mar 11, 2024

11/03/2034

09/18/2025 19:00:01

RAPID SARS-CoV-2 ANTIGEN TEST CARD
Risk Class III

Registration Details

80313210031

25351758805202391

07776689000190

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Mar 11, 2024

11/03/2034

09/18/2025 19:00:01