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Kerecis Omega3 Wound

by Kerecis Limited Iceland EUDAMED

Ref 50200S01B0B EMDN M04041001

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-50200S01AK Basic UDI-DIDate29 Mar 2022RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Kerecis™ Omega3 Wound
Model / Reference
50200S01B0B
Primary DI / UDI-DI
D-50200S01AK
Basic UDI-DI
B-50200S01AK
EMDN Code
M04041001 Animal-derived collagen dressings, non-combined
Device Class
Class III
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
IS-MF-000001365

Other devices from Kerecis

See all devices from Kerecis →

Properties & raw data

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

Sources (1)

  • EUDAMED 0546a4b6-41f9-4871-8151-3a61a3f0fee3 61 fields · synced 24 Oct 2026