HUMAN PAPILLOMAVIRUS (HPV) - ANVISA Registration 82149920118
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 82149920118 and manufactured by CERTEST BIOTEC, S.L.. The registration is held by GENESTAR INOVAÇÕES E EQUIPAMENTOS MÉDICOS LTDA with validity until May 19, 2035.
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
82149920118
25351412848202412
35489323000175
Company Information
Dates and Status
May 19, 2025
19/05/2035
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)
Kit Detecção qPCR para HPV de Alto Risco 2 Genotipados e 13 Detectados
SANSURE BIOTECH INC
80680250055
Apr 28, 2025

