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Willospon®

by Will-Pharma BV Netherlands EUDAMED

Ref 20925NL-1

EMDN M040503

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08712691209205 Basic UDI-DIDate27 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Willospon Standard 8 x 5 x 1 cm
Model / Reference
20925NL-1
Primary DI / UDI-DI
08712691209205
Basic UDI-DI
B-08712691209205
EMDN Code
M040503 Gelatine sponge haemostatic dressings
Device Class
Class III
Market of Registration
Belgium

Manufacturer details

EUDAMED SRN
NL-MF-000006884

Other devices from Will-Pharma BV

See all devices from Will-Pharma BV →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Implantable
  • Animal Tissues
Other properties (8)
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 870aacef-5707-4747-898f-9addb899e0c3 61 fields · synced 22 Oct 2026