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TissuePatchDural

by Tissuemed Limited 4 variants

Ref TD-02Model TissuePatchDural

Active European Union

CE MDD

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-0506019320005LBE Basic UDI-DI D-0506019320005LBEUDI-DIDate20 Oct 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
TissuePatch Dural Sealant Film
Model / Reference
TissuePatchDural, TD-02
Primary DI / UDI-DI
D-0506019320005LBE
Basic UDI-DI
B-0506019320005LBE
EMDN Code
H900199 Tissue adhesives - other
Device Class
Class III
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
GB-MF-000011031
Authorised representative
Becton Dickinson Ireland Limited IE-AR-000007610

Other devices from Tissuemed Limited

See all devices from Tissuemed Limited →

Properties

  • Sterile
  • Implantable

Other properties (11)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No