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Heat Pads

by Henan Kangdi Medical Devices Co., Ltd. 9 variants

Model 10x20cm,10x13cm,7.4x11.2cm,7x9cm,9.6x12.8cm,5.5x9.2cm

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69505629Hp000013059RZ Basic UDI-DI 06950562984031UDI-DIDate18 Jun 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
10x20cm, 10x13cm, 7.4x11.2cm, 7x9cm, 9.6x12.8cm, 5.5x9.2cm
Primary DI / UDI-DI
06950562984031
Basic UDI-DI
69505629Hp000013059RZ
EMDN Code
Z120602 Physiotherapy equipment
Device Class
Class IIa
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000013059
Authorised representative
Luxus Lebenswelt GmbH DE-AR-000005110

Other devices from Henan Kangdi Medical Devices Co., Ltd.

See all devices from Henan Kangdi Medical Devices 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