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Duk-In Lite 'S'

by Duk-In Co., Ltd. 4 variants

Ref L4154Model Cast

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number88000337LITE100G2 Basic UDI-DI 08800033700159UDI-DIDate14 Jun 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Synthetic Orthopedic Casting Tape
Model / Reference
Cast, L4154
Primary DI / UDI-DI
08800033700159
Basic UDI-DI
88000337LITE100G2
Direct Marketing DI
08800033700159
EMDN Code
M03050202 Synthetic cast bandages and splints
Device Class
Class I
EU market of registration
Malta

Manufacturer details

EUDAMED SRN
KR-MF-000026961
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Duk-In Co., Ltd.

See all devices from Duk-In Co., Ltd. →

Properties

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