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Spongostan™

by Ferrosan Medical Devices A/S Denmark EUDAMED

Ref MS0008

EMDN M040599

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-25712123000780 Basic UDI-DIDate25 Apr 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 23 Oct 2026

Device Name
SPONGOSTAN™ Absorbable Haemostatic Gelatin Powder
Model / Reference
MS0008
Primary DI / UDI-DI
25712123000780
Basic UDI-DI
B-25712123000780
EMDN Code
M040599 Haemostatic dressings - other
Device Class
Class III
Market of Registration
Denmark

Manufacturer details

EUDAMED SRN
DK-MF-000002856

Other devices from Ferrosan Medical Devices A/S

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Animal Tissues
Other properties (9)
  • Implantable: No
  • 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 291f1074-9807-4271-a9aa-40bdaa8c2246 61 fields · synced 23 Oct 2026