ANVISA registration

AMNIOSCÓPIO MANUAL RSP HOSPITALAR

Registration 81094800009. Amnioscopio

Registration details

Registration number81094800009
Application number25351741918201416
Technical nameAmnioscopio
Risk classI
Published on02/03/2015
ValidityIndefinite validity

Registration holder

Legal nameORTOFEX INDÚSTRIA E COMÉRCIO DE APARELHOS MÉDICOS E ORTOPÉDICOS LTDA.-ME
CNPJ19.973.704/0001-79

Manufacturer

  • ORTOFEX INDÚSTRIA E COMÉRCIO DE APARELHOS MÉDICOS E ORTOPÉDICOS LTDA.-ME BRASIL

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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Medical device registration with ANVISA

HSC manages the process from risk classification to liaising with the regulator, in Brazil and more than 40 other countries.

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