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Aurobond

by Aurolab

Ref NilModel E5101,E5102,E2202,E2204,E4101,E4102

Aurobond (Nil) is a Class IIb device made by Aurolab, registered in EUDAMED on 14 Oct 2026 (Basic UDI-DI B-803878PE0001XZS5), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-803878PE0001XZS5 Basic UDI-DI D-803878PE0001XZS5UDI-DIDate14 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Non absorbable ophthalmic suture with needles
Model / reference
E5101, E5102, E2202, E2204, E4101, E4102, Nil
Primary DI / UDI-DI
D-803878PE0001XZS5
Basic UDI-DI
B-803878PE0001XZS5
EMDN code
H010201020201 Polyester multifilament with needle for open surgery
Device class
Class IIb
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

Similar devices in this category

Other devices filed under POLYESTER MULTIFILAMENT WITH NEEDLE FOR OPEN SURGERY.

Other devices from Aurolab

See all devices from Aurolab →

Properties

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