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HUMAN PAPILLOMAVIRUS (HPV) - ANVISA Registration 80102513036

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 80102513036 and manufactured by SEEGENE INC.. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Jun 19, 2033.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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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80102513036
2 Related Devices
Registration Details
ANVISA Registration Number: 80102513036
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Related Devices (2)

AllplexTM HPV HR Detection
Risk Class III

Registration Details

80102513036

25351393568202228

04718143000194

Company Information

SEEGENE INC.
South Korea
PT: CORÉIA DO SUL

Dates and Status

Jun 19, 2023

19/06/2033

09/18/2025 19:00:01

AllplexTM HPV HR Detection
Risk Class III

Registration Details

80102513036

25351393568202228

04718143000194

Dates and Status

Jun 19, 2023

19/06/2033

09/18/2025 19:00:01