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YELLOW FEVER - ANVISA Registration 80780040002

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 80780040002 and manufactured by INSTITUTO DE BIOLOGIA MOLECULAR DO PARANÁ. The registration is held by INSTITUTO DE BIOLOGIA MOLECULAR DO PARANÁ with validity until Aug 24, 2030.

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.

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80780040002
Registration Details
ANVISA Registration Number: 80780040002
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Device Details

Kit IBMP Biomol Febre Amarela
Risk Class III

Registration Details

80780040002

25351453605202001

03585986000105

Company Information

Brazil
PT: BRASIL

Dates and Status

Aug 24, 2020

24/08/2030

09/18/2025 19:00:01