CORONAVIRUS - ANVISA Registration 80954880138

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 80954880138 and manufactured by manufacturer not specified. The registration is held by Eco Diagnostica Ltda with validity until Jul 09, 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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80954880138
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Registration Details
ANVISA Registration Number: 80954880138
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

STANDARD Q COVID-19 IgM/IgG Combo Test
Risk Class III

Registration Details

80954880138

25351421278202010

14633154000206

Company Information

Dates and Status

Jul 09, 2020

09/07/2030

09/18/2025 19:00:01

STANDARD Q COVID-19 IgM/IgG Combo Test
Risk Class III

Registration Details

80954880138

25351421278202010

14633154000206

Company Information

SD BIOSENSOR, INC.
South Korea
PT: CORÉIA DO SUL

Dates and Status

Jul 09, 2020

09/07/2030

09/18/2025 19:00:01