CORONAVIRUS - ANVISA Registration 80885650042

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 80885650042 and manufactured by manufacturer not specified. The registration is held by ORBITAE DIAGNOSTICOS LTDA with validity until Mar 08, 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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80885650042
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Registration Details
ANVISA Registration Number: 80885650042
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

GENEDIA W ONE COVID-19 IgM/IgG
Risk Class III

Registration Details

80885650042

25351000872202151

11162384000165

Company Information

Dates and Status

Mar 08, 2021

08/03/2031

09/18/2025 19:00:01

GENEDIA W ONE COVID-19 IgM/IgG
Risk Class III

Registration Details

80885650042

25351000872202151

11162384000165

Company Information

South Korea
PT: CORÉIA DO SUL

Dates and Status

Mar 08, 2021

08/03/2031

09/18/2025 19:00:01