CORONAVIRUS - ANVISA Registration 81268670005

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 81268670005 and manufactured by manufacturer not specified. The registration is held by ONEWAY IMPORTADORA E DISTRIBUIDORA LTDA with validity until Jun 01, 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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81268670005
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Registration Details
ANVISA Registration Number: 81268670005
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

QuickProfile® 2019-nCoV IgG/IgM Combo Test Card
Risk Class III

Registration Details

81268670005

25351382010202055

13605812000102

Company Information

Dates and Status

Jun 01, 2020

01/06/2030

09/18/2025 19:00:01

QuickProfile® 2019-nCoV IgG/IgM Combo Test Card
Risk Class III

Registration Details

81268670005

25351382010202055

13605812000102

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jun 01, 2020

01/06/2030

09/18/2025 19:00:01