HUMAN PAPILLOMAVIRUS (HPV) - ANVISA Registration 80502070111

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 80502070111 and manufactured by VITRO SA. The registration is held by MOBIUS LIFE SCIENCE INDUSTRIA E COMERCIO DE PRODUTOS PARA LABORATORIOS LTDA with validity until Aug 07, 2033.

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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80502070111
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Registration Details
ANVISA Registration Number: 80502070111
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

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Related Devices (2)

Família Master HPV Alto Risco
Risk Class III

Registration Details

80502070111

25351558357202247

04645160000149

Company Information

VITRO SA
Spain
PT: ESPANHA

Dates and Status

Aug 07, 2023

07/08/2033

09/18/2025 19:00:01

Família Master HPV Alto Risco
Risk Class III

Registration Details

80502070111

25351558357202247

04645160000149

Dates and Status

Aug 07, 2023

07/08/2033

09/18/2025 19:00:01