HUMAN PAPILLOMAVIRUS (HPV) - ANVISA Registration 81325990319

Access comprehensive regulatory information for HUMAN PAPILLOMAVIRUS (HPV) in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81325990319 and manufactured by manufacturer not specified. The registration is held by QR CONSULTING, IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDA with validity until Jan 08, 2034.

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 GENOMICA S.A.U., MOBIUS LIFE SCIENCE INDÚSTRIA E COMERCIO DE PRODUTOS PARA LABORATÓRIOS 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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81325990319
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Registration Details
ANVISA Registration Number: 81325990319
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Família Kit de Teste de Amplificação de Ácido Nucléico de Papilomavírus Humano
Risk Class III

Registration Details

81325990319

25351547116202353

19933144000129

Dates and Status

Jan 08, 2024

08/01/2034

09/18/2025 19:00:01

Família Kit de Teste de Amplificação de Ácido Nucléico de Papilomavírus Humano
Risk Class III

Registration Details

81325990319

25351547116202353

19933144000129

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Jan 08, 2024

08/01/2034

09/18/2025 19:00:01