CORONAVIRUS - ANVISA Registration 81062710051

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 81062710051 and manufactured by manufacturer not specified. The registration is held by Cepheid Brasil Importação, Exportação e Comércio de Produtos de Diagnósticos ltda with validity until Dec 26, 2032.

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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81062710051
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Registration Details
ANVISA Registration Number: 81062710051
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Xpert Xpress CoV-2 plus
Risk Class III

Registration Details

81062710051

25351133566202281

18628083000123

Dates and Status

Dec 26, 2022

26/12/2032

09/18/2025 19:00:01

Xpert Xpress CoV-2 plus
Risk Class III

Registration Details

81062710051

25351133566202281

18628083000123

Company Information

CEPHEID
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Dec 26, 2022

26/12/2032

09/18/2025 19:00:01