CORONAVIRUS - ANVISA Registration 80537410093

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 80537410093 and manufactured by manufacturer not specified. The registration is held by CELER BIOTECNOLOGIA S/A with validity until Apr 19, 2031.

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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80537410093
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Registration Details
ANVISA Registration Number: 80537410093
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Celer Wondfo SARS-CoV-2 Anticorpo RBD Rapid Test
Risk Class III

Registration Details

80537410093

25351040879202114

04846613000103

Company Information

Dates and Status

Apr 19, 2021

19/04/2031

09/18/2025 19:00:01

Celer Wondfo SARS-CoV-2 Anticorpo RBD Rapid Test
Risk Class III

Registration Details

80537410093

25351040879202114

04846613000103

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Apr 19, 2021

19/04/2031

09/18/2025 19:00:01