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Anika

by Novavision Group Italy EUDAMED

Ref 380800000335Model Carboxytherapy Medical Device

EMDN Z12029008

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08059340930012 Basic UDI-DIDate28 Nov 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Novaclinical Anika
Model / Reference
Carboxytherapy Medical Device, 380800000335
Primary DI / UDI-DI
08059340930012
Basic UDI-DI
B-08059340930012, 805934093N011848
Direct Marketing DI
08059340930012
EMDN Code
Z12029008, Z12040299
Device Class
Class IIb
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000024333

Other devices from Novavision Group

See all devices from Novavision Group →

Properties & raw data

Show properties, registry sources and raw records
Other properties (13)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (2)

  • EUDAMED 3e3ca421-b31c-4be7-818d-35cb6a1b2e96 61 fields · synced 22 Oct 2026
  • EUDAMED 08059340930012|805934093N011848 61 fields · synced 19 May 2026