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CuraSpon Standard

by CuraMedical B.V. Netherlands EUDAMED

Ref CS-010

EMDN M040503

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08717903340103 Basic UDI-DIDate17 Aug 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 24 Oct 2026

Device Name
CuraSpon Standard
Model / Reference
CS-010
Primary DI / UDI-DI
08717903340103
Basic UDI-DI
B-08717903340103
EMDN Code
M040503 Gelatine sponge haemostatic dressings
Device Class
Class III
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
NL-MF-000000052

Other devices from CuraMedical B.V.

See all devices from CuraMedical B.V. →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Implantable
  • Animal Tissues
Other properties (10)
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 80339ac8-fd2d-4dcb-96f5-deb6e6e1d3c1 61 fields · synced 24 Oct 2026