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Aurooctane

by Aurolab

Ref Nil

Aurooctane (Nil) is a Class IIa device made by Aurolab, registered in EUDAMED on 13 Oct 2026 (Basic UDI-DI B-803878AO0001VCLW), active as of 24 Oct 2026.

Active European Union

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-803878AO0001VCLW Basic UDI-DI D-803878AO0001VCLWUDI-DIDate13 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Perfluoro-n-octane
Model / reference
Nil
Primary DI / UDI-DI
D-803878AO0001VCLW
Basic UDI-DI
B-803878AO0001VCLW
EMDN code
Q02030205 Ophthalmic surgery, perfluorocarbons pure and combined with other substances
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Denmark

Manufacturer details

EUDAMED SRN
IN-MF-000007255
Authorised representative
mdi Europa GmbH DE-AR-000006218

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Properties

  • Supplied sterile
Other properties (11, all answered No)