HUMAN PAPILLOMAVIRUS (HPV) - ANVISA Registration 80680250055
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 80680250055 and manufactured by SANSURE BIOTECH INC. The registration is held by STRA NEGOCIOS EM SAUDE E BEM ESTAR LTDA with validity until Apr 28, 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
80680250055
25351446659202435
11388997000115
Company Information
Dates and Status
Apr 28, 2025
28/04/2035
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)
VIASURE High-Risk Human Papilloma Virus Real Time PCR Detection Kit
CERTEST BIOTEC, S.L.
82149920118
May 19, 2025

