ANVISA registration

KIT INSTRUMENTAL REVISÃO HASTE FEMORAL PROVA DE PESCOÇO DE HASTE 9038.21.000

Registration 80070180076. Kit Instrumental

Registration details

Registration number80070180076
Application number25351016773201977
Technical nameKit Instrumental
Risk classI
Published on01/04/2019
ValidityIndefinite validity

Registration holder

Legal nameENOVIS SURGICAL BRASIL LTDA
CNPJ03.117.039/0001-81

Manufacturer

  • Limacorporate S.p.A ITÁLIA

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