CORONAVIRUS - ANVISA Registration 80804670001

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 80804670001 and manufactured by HUMASIS CO. LTD.. The registration is held by CELLTRION HEALTHCARE DISTRIBUICAO DE PRODUTOS FARMACEUTICOS DOS BRASIL LTDA with validity until Oct 25, 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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80804670001
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Registration Details
ANVISA Registration Number: 80804670001
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Celltrion DiaTrust(TM) COVID-19 igG/IgM Rapid Test
Risk Class III

Registration Details

80804670001

25351905204202031

05452889000161

Company Information

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

Dates and Status

Oct 25, 2021

25/10/2031

09/18/2025 19:00:01

Celltrion DiaTrust(TM) COVID-19 igG/IgM Rapid Test
Risk Class III

Registration Details

80804670001

25351905204202031

05452889000161

Dates and Status

Oct 25, 2021

25/10/2031

09/18/2025 19:00:01