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

YELLOW FEVER - ANVISA Registration 80780040025

Access comprehensive regulatory information for YELLOW FEVER in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80780040025 and manufactured by INSTITUTO DE BIOLOGIA MOLECULAR DO PARANÁ. The registration is held by INSTITUTO DE BIOLOGIA MOLECULAR DO PARANÁ with validity until May 19, 2035.

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including FUNDAÇÃO BAIANA DE PESQ. CIENTIFICA E DESENV. TECNOLOGICO, FORNECIMENTO E DISTRIBUIÇÃO DE MEDICAMENTOS-BAHIAFARMA, FUNDAÇÃO OSWALDO CRUZ, 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
80780040025
Registration Details
ANVISA Registration Number: 80780040025
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Kit IBMP Biomol Febre Amarela One
Risk Class III

Registration Details

80780040025

25351463003202487

03585986000105

Company Information

Brazil
PT: BRASIL

Dates and Status

May 19, 2025

19/05/2035

09/18/2025 19:00:01