CORONAVIRUS - ANVISA Registration 80638720162

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 80638720162 and manufactured by HUMASIS CO., LTD. The registration is held by DIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - ME with validity until Sep 10, 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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80638720162
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Registration Details
ANVISA Registration Number: 80638720162
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

COVID-19 AG RAPID TEST
Risk Class III

Registration Details

80638720162

25351899754202012

11462456000190

Company Information

HUMASIS CO., LTD
South Korea
PT: CORÉIA DO SUL

Dates and Status

Sep 10, 2020

10/09/2030

09/18/2025 19:00:01

COVID-19 AG RAPID TEST
Risk Class III

Registration Details

80638720162

25351899754202012

11462456000190

Company Information

Dates and Status

Sep 10, 2020

10/09/2030

09/18/2025 19:00:01