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Blood and Infusion Warmer

by Beijing KellyMed Co., Ltd. 2 variants

Ref KL-2031NModel KL-2031N, KL-2032N

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69532515HT001KC Basic UDI-DI 06953251540013UDI-DIDate20 Jul 2026RegisteredStatusActive

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  • Withdrawn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
Blood and Infusion Warmer
Model / Reference
KL-2031N, KL-2032N
Primary DI / UDI-DI
06953251540013
Basic UDI-DI
69532515HT001KC
Direct Marketing DI
06953251540013
EMDN Code
Z12030305 Infusion heaters
Device Class
Class IIa
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
CN-MF-000017305
Authorised representative
Umedwings Netherlands B.V. NL-AR-000000444

Other devices from Beijing KellyMed Co., Ltd.

See all devices from Beijing KellyMed 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