ANVISA registration

FLEXPRO PENMATE

Registration 82113060001. Dispositivo Para Fobia de Agulha

Registration details

Registration number82113060001
Application number25351205038202401
Technical nameDispositivo Para Fobia de Agulha
Risk classI
Published on06/05/2024
ValidityIndefinite validity

Registration holder

Legal nameNOVO NORDISK FARMACÊUTICA DO BRASIL LTDA
CNPJ82.277.955/0007-40

Manufacturer

  • NOVO NORDISK A/S DINAMARCA

Source: ANVISA

Source: ANVISA open data, medical device file, updated daily. The public database provides registration validity, rather than registration status: this registration may have been cancelled before its expiry date without this being shown here. Before making purchasing, import or marketing decisions, check the ANVISA search portal.

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