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Warming Profile

by Keewell Medical Technology Co., Ltd EUDAMED

Active European Union

Ref I.D. 6.5mmModel I.D. 3.5mm, I.D. 6.5mm, I.D. 9.5mm, I.D. 14.5mm

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69542183QH001M9 Basic UDI-DIDate2 Jul 2022RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Model / Reference
I.D. 3.5mm, I.D. 6.5mm, I.D. 9.5mm, I.D. 14.5mm
Primary DI / UDI-DI
06954218311028
Basic UDI-DI
69542183QH001M9
EMDN Code
Z12030380 Infusion instruments - hardware accessories
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000016265
Authorised representative
Wellita International BV BE-AR-000010384

Other devices from Keewell Medical Technology Co., Ltd

See all devices from Keewell Medical Technology Co., Ltd →

Properties

Show 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