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Granudacyn

by P.G.F. Industry Solutions GmbH 13 variants

Ref 360108Model 100 g Spray

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-09120073781062 Basic UDI-DI 09120073781062UDI-DIDate17 Feb 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  • Withdrawn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
Granudacyn Wundgel
Model / Reference
100 g Spray, 360108
Primary DI / UDI-DI
09120073781062
Basic UDI-DI
B-09120073781062
EMDN Code
M040499 Dressings for wounds, sores and ulcerations - other
Device Class
Class IIb
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
AT-MF-000000310

Other devices from P.G.F. Industry Solutions GmbH

See all devices from P.G.F. Industry Solutions GmbH →

Properties

  • Incorporates Medicinal Product

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No