ANVISA registration

KIT DE CATETERIZAÇÃO VENOSA CENTRAL DUPLO LÚMEN PEDIÁTRICO

Registration 80312270048. Cateteres

Registration details

Registration number80312270048
Application number25351037862202503
Technical nameCateteres
Risk classIV
Published on04/08/2025
ValidityValid until 16/09/2029

Registration holder

Legal nameTELEFLEX MEDICAL BRASIL LTDA
CNPJ06.089.071/0001-99

Manufacturer

  • ARROW INTERNATIONAL LLC (SUBSIDIARY OF TELEFLEX INCORPORATED) ESTADOS UNIDOS DA AMÉRICA

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.

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