Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
82149920118
2 Related Devices
Registration Details
ANVISA Registration Number: 82149920118
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Related Devices (2)

VIASURE High-Risk Human Papilloma Virus Real Time PCR Detection Kit
Risk Class III

Registration Details

82149920118

25351412848202412

35489323000175

Company Information

Spain
PT: ESPANHA

Dates and Status

May 19, 2025

19/05/2035

09/18/2025 19:00:01

VIASURE High-Risk Human Papilloma Virus Real Time PCR Detection Kit
Risk Class III

Registration Details

82149920118

25351412848202412

35489323000175

Company Information

Dates and Status

May 19, 2025

19/05/2035

09/18/2025 19:00:01