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CORONAVIRUS - ANVISA Registration 80524900076

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 80524900076 and manufactured by manufacturer not specified. The registration is held by BIO ADVANCE DIAGNOSTICOS LTDA with validity until Dec 21, 2030.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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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80524900076
2 Related Devices
Registration Details
ANVISA Registration Number: 80524900076
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Related Devices (2)

Teste Rápido OnSite Covid-19 Ag
Risk Class III

Registration Details

80524900076

25351540508202049

09593438000103

Company Information

Dates and Status

Dec 21, 2020

21/12/2030

09/18/2025 19:00:01

Teste Rápido OnSite Covid-19 Ag
Risk Class III

Registration Details

80524900076

25351540508202049

09593438000103

Company Information

CTK BIOTECH, INC.
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Dec 21, 2020

21/12/2030

09/18/2025 19:00:01