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Plaque Disclosing Agent - ANVISA Registration 80013980039

Access comprehensive regulatory information for Plaque Disclosing Agent in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80013980039 and manufactured by F & A LABORATÓRIO FARMACÊUTICO LTDA-ME. The registration is held by F & A LABORATÓRIO FARMACÊUTICO LTDA-ME with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including F & A LABORATÓRIO FARMACÊUTICO LTDA-ME, AAF DO BRASIL PRODUTOS ODONTOLOGICOS 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.

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80013980039
Registration Details
ANVISA Registration Number: 80013980039
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Device Details

FLÚOR ESPUMA - FÓMULA & AÇÃO
Risk Class I

Registration Details

80013980039

25351587436201960

01953085000195

Company Information

Brazil
PT: BRASIL

Dates and Status

Oct 17, 2019

VIGENTE

09/18/2025 19:00:01