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Polygreen

by K-jump Health Co., Ltd. 11 variants

Ref KD-153Model KD-112

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42520106KD0115RS Basic UDI-DI 04252010615309UDI-DIDate29 Jul 2025RegisteredStatusActive

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  • Withdrawn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

Device Name
clinical electronic thermometer
Model / Reference
KD-112, KD-153
Primary DI / UDI-DI
04252010615309
Basic UDI-DI
42520106KD0115RS, B-04252010615309
Direct Marketing DI
04252010615309
EMDN Code
V0301010201 Contact digital thermometers (including probes)
Device Class
Class IIa
EU market of registration
Germany
France

Manufacturer details

EUDAMED SRN
TW-MF-000020665
Authorised representative
Polygreen Germany GmbH DE-AR-000019484

Other devices from K-jump Health Co., Ltd.

See all devices from K-jump Health Co., Ltd. →

Properties

  • Measuring Function

Other properties (12)

  • 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
  • Incorporates Medicinal Product: No