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Aurosling

by Aurolab

Ref NilModel T9052

Aurosling (Nil) is a Class IIb device made by Aurolab, registered in EUDAMED on 13 Oct 2026 (Basic UDI-DI B-803878PT000159UW), 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-803878PT000159UW Basic UDI-DI D-803878PT000159UWUDI-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  • Withdrawn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
Ptosis Sling
Model / reference
T9052, Nil
Primary DI / UDI-DI
D-803878PT000159UW
Basic UDI-DI
B-803878PT000159UW
EMDN code
H0199 Surgical sutures - other
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 SURGICAL SUTURES.

Other devices from Aurolab

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Properties

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