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creos™ xenoform

by Chiyewon Co., LTD. EUDAMED

Active European Union

Ref CHY25-1217

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08809490623544 Basic UDI-DIDate22 Jan 2026RegisteredStatusActive

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  • Withdrawn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

Model / Reference
CHY25-1217
Primary DI / UDI-DI
08809490623544
Basic UDI-DI
B-08809490623544
EMDN Code
Q010302 Dental graft devices
Device Class
Class III
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
KR-MF-000022264
Authorised representative
Obelis s.a. BE-AR-000000106

Other devices from Chiyewon Co., LTD.

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Properties

  • 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