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Oroben Mundgel

by Aboca S.P.A. Società Agricola EUDAMED

Active European Union

Ref ATOROGLX/DEOROGLX

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-ITM29499ATOROGLXYP Basic UDI-DIDate4 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Oroben Gel Orale
Model / Reference
ATOROGLX/DEOROGLX
Primary DI / UDI-DI
D-ITM29499ATOROGLXYP
Basic UDI-DI
B-ITM29499ATOROGLXYP
EMDN Code
V9017 Oral administration preparations not included in other classes
Device Class
Class IIa
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
IT-MF-000029499

Other devices from Aboca S.P.A. Società Agricola

See all devices from Aboca S.P.A. Società Agricola →

Properties

Show properties
Other properties (11)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No