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Aadi

by Aurolab

Ref NilModel AADI - 350

Aadi (Nil) is a Class IIb device made by Aurolab, registered in EUDAMED on 13 Oct 2026 (Basic UDI-DI B-803878GS0001Z6S8), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-803878GS0001Z6S8 Basic UDI-DI D-803878GS0001Z6S8UDI-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  • Withdrawn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
Glaucoma Shunt
Model / reference
AADI - 350, Nil
Primary DI / UDI-DI
D-803878GS0001Z6S8
Basic UDI-DI
B-803878GS0001Z6S8
EMDN code
Q0208 Glaucoma drainages and kits
Device class
Class IIb
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

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

Similar devices in this category

Other devices filed under GLAUCOMA DRAINAGES AND KITS.

Other devices from Aurolab

See all devices from Aurolab →

Properties

  • Supplied sterile
  • Implantable
Other properties (10, all answered No)