Skip to content

Modibuck Percussion Hammer

by Chin Kou Medical Instrument Co., Ltd. Taiwan EUDAMED

Ref CK-505 Model CK-501

EMDN L160101

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number471989020PHCK5XXT8 Basic UDI-DIDate1 Jul 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 25 Oct 2026

Device Name
Percussion Hammer
Model / Reference
CK-501, CK-505
Primary DI / UDI-DI
04719890205056
Basic UDI-DI
471989020PHCK5XXT8
EMDN Code
L160101 Neurological hammers, reusable
Device Class
Class I
Market of Registration
Poland

Manufacturer details

EUDAMED SRN
TW-MF-000042725
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Chin Kou Medical Instrument Co., Ltd.

See all devices from Chin Kou Medical Instrument Co., Ltd. →

Properties & raw data

Show properties, registry sources and raw records
Other properties (13)
  • Sterile: No
  • Implantable: No
  • 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 04719890205056|471989020PHCK5XXT8 61 fields · synced 25 Oct 2026