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.
Related Devices (2)
Registration Details
80102513036
25351393568202228
04718143000194
Company Information
Dates and Status
Jun 19, 2023
19/06/2033
09/18/2025 19:00:01
PAPILOMAVÍRUS HUMANO (HPV)
Truenat® HPV-HR
Not specified
82807480006
Jun 02, 2025
PAPILOMAVÍRUS HUMANO (HPV)
Truenat® HPV-HR
MOLBIO DIAGNOSTICS LIMITED
82807480006
Jun 02, 2025
PAPILOMAVÍRUS HUMANO (HPV)
VIASURE High-Risk Human Papilloma Virus Real Time PCR Detection Kit com Controle de Extração.
Not specified
82149920117
May 19, 2025
PAPILOMAVÍRUS HUMANO (HPV)
VIASURE High-Risk Human Papilloma Virus Real Time PCR Detection Kit com Controle de Extração.
CERTEST BIOTEC, S.L.
82149920117
May 19, 2025
PAPILOMAVÍRUS HUMANO (HPV)
VIASURE High-Risk Human Papilloma Virus Real Time PCR Detection Kit
CERTEST BIOTEC, S.L.
82149920118
May 19, 2025

