CORONAVIRUS - ANVISA Registration 10350840368

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 10350840368 and manufactured by BODITECH MED INCORPORATED. The registration is held by BIOSYS LTDA with validity until Jul 13, 2030.

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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10350840368
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Registration Details
ANVISA Registration Number: 10350840368
Janaina dos Santos de Miranda

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Related Devices (2)

Família AFIAS COVID-19 Ag
Risk Class III

Registration Details

10350840368

25351603810202015

02220795000179

Company Information

South Korea
PT: CORÉIA DO SUL

Dates and Status

Jul 13, 2020

13/07/2030

09/18/2025 19:00:01

Família AFIAS COVID-19 Ag
Risk Class III

Registration Details

10350840368

25351603810202015

02220795000179

Company Information

Dates and Status

Jul 13, 2020

13/07/2030

09/18/2025 19:00:01