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TENS Electrode Pads

by Boen Healthcare Co., Ltd

Ref 204602Model 4x4cm, 5x5cm, 5x9cm, 5x10cm, dia. 22mm, dia. 25mm, dia. 30mm

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69241056TENSSZ Basic UDI-DI 06924105635612UDI-DIDate24 Jun 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  • Withdrawn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
Self-adhesive Electrodes
Model / Reference
4x4cm, 5x5cm, 5x9cm, 5x10cm, dia. 22mm, dia. 25mm, dia. 30mm, 204602
Primary DI / UDI-DI
06924105635612
Basic UDI-DI
69241056TENSSZ
Direct Marketing DI
06924105635612
EMDN Code
N010201 Tens system electrodes
Device Class
Class I
EU market of registration
Lithuania

Manufacturer details

EUDAMED SRN
CN-MF-000040773
Authorised representative
Everbiz GmbH AT-AR-000035279

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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