ANVISA registration

Kit Cânula de Discectomia Percutânea Lombar Uniomaxx

Registration 82209529178. Kit Instrumental

Registration details

Registration number82209529178
Application number25351215999202335
Technical nameKit Instrumental
Risk classII
Published on24/04/2023
ValidityIndefinite validity

Registration holder

Legal nameMARDEN MEDICAL LTDA
CNPJ40.220.751/0001-38

Manufacturer

  • MARDEN MEDICAL 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.

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