ANVISA registration

URETEROSCÓPIO FLEXÍVEL DIGITAL SCIVITA

Registration 80082919041. Endoscopio Flexivel

Registration details

Registration number80082919041
Application number25351397766202422
Technical nameEndoscopio Flexivel
Risk classII
Published on30/09/2024
ValidityIndefinite validity

Registration holder

Legal nameCIENLABOR INDUSTRIA E COMERCIO LTDA
CNPJ02.814.280/0001-05

Manufacturer

  • SCIVITA MEDICAL TECHNOLOGY CO., LTD. CHINA, REPÚBLICA POPULAR

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