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Adherus

by Stryker Leibinger GmbH & Co.KG 3 variants

Ref NUS-009-01

Adherus (NUS-009-01) is a Class III device made by Stryker Leibinger GmbH & Co.KG, registered in EUDAMED on 26 Oct 2026 (Basic UDI-DI B-07613327697452), active as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-07613327697452 Basic UDI-DI 07613327697452UDI-DIDate26 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Adherus AutoSpray ET Dural Sealant
Model / reference
NUS-009-01
Primary DI / UDI-DI
07613327697452
Basic UDI-DI
B-07613327697452
EMDN code
H90010102 Synthetic glues
Device class
Class III
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005522

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Other devices filed under SYNTHETIC GLUES.

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Properties

  • Supplied sterile
  • Implantable
Other properties (12, all answered No)