HUMAN PAPILLOMAVIRUS (HPV) - ANVISA Registration 10287410898

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 10287410898 and manufactured by ROCHE MOLECULAR SYSTEMS, INC. The registration is held by ROCHE DIAGNÓSTICA BRASIL LTDA with validity until Oct 04, 2035.

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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10287410898
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Registration Details
ANVISA Registration Number: 10287410898
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

cobas® 4800 HPV - Amplification/Detection Kit
Risk Class III

Registration Details

10287410898

25351414690201045

30280358000186

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Oct 04, 2010

04/10/2035

09/18/2025 19:00:01

cobas® 4800 HPV - Amplification/Detection Kit
Risk Class III

Registration Details

10287410898

25351414690201045

30280358000186

Company Information

Dates and Status

Oct 04, 2010

04/10/2035

09/18/2025 19:00:01