Skip to content

NORDEPLAST Kinesio tape 5 cm × 5 m (BEIGE)

by Liepājas Speciālās ekonomiskās zonas SIA NordePlast

Ref REF535970

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4752256KT200726F5 Basic UDI-DI 04751028535970UDI-DIDate5 Oct 2026RegisteredStatusActive

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  • Withdrawn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
Kinesio tape
Model / Reference
REF535970
Primary DI / UDI-DI
04751028535970
Basic UDI-DI
4752256KT200726F5
EMDN Code
M030402030102 Elastic support bandages, adhesive extensible in one direction, high extensibility
Device Class
Class I
EU market of registration
Latvia

Manufacturer details

EUDAMED SRN
LV-MF-000026735

Other devices from Liepājas Speciālās ekonomiskās zonas SIA NordePlast

See all devices from Liepājas Speciālās ekonomiskās zonas SIA NordePlast →

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