Skip to content

CuraCel Fibrillar

by CuraMedical B.V. Netherlands EUDAMED

Ref CF-738

EMDN M040501

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08717903347386 Basic UDI-DIDate24 Nov 2021RegisteredStatusActive

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
CuraCel Fibrillar
Model / Reference
CF-738
Primary DI / UDI-DI
08717903347386
Basic UDI-DI
B-08717903347386
EMDN Code
M040501 Polysaccharide 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
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

Sources (1)

  • EUDAMED d2411179-cec1-4170-9329-b2d95edaef40 61 fields · synced 24 Oct 2026