CORONAVIRUS - ANVISA Registration 82228590001

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 82228590001 and manufactured by manufacturer not specified. The registration is held by JA CORPORATION LTDA with validity until May 16, 2032.

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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82228590001
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Registration Details
ANVISA Registration Number: 82228590001
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

JA Wondfo CoV 2 Ag Rapid Test.
Risk Class III

Registration Details

82228590001

25351129595202249

23632619000114

Company Information

Dates and Status

May 16, 2022

16/05/2032

09/18/2025 19:00:01

JA Wondfo CoV 2 Ag Rapid Test.
Risk Class III

Registration Details

82228590001

25351129595202249

23632619000114

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

May 16, 2022

16/05/2032

09/18/2025 19:00:01