ANVISA registration

Reanimador Manual (Ambu) Romed

Registration 81284390011. Ressuscitador Cardio-Pulmonar

Registration details

Registration number81284390011
Application number25351337605201609
Technical nameRessuscitador Cardio-Pulmonar
Risk classII
Published on31/10/2016
ValidityIndefinite validity

Registration holder

Legal nameROMED INDÚSTRIA E COMÉRCIO DE EQUIPAMENTOS MÉDICOS LTDA
CNPJ13.644.713/0001-30

Manufacturer

  • ROMED INDÚSTRIA E COMÉRCIO DE EQUIPAMENTOS MÉDICOS LTDA 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.

Next step

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.

Speak to a specialist