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Forced-Air Warming Blankets

by Keewell Medical Technology Co., Ltd EUDAMED

Active European Union

Ref KWB011, KWB0172, KWB0181, KWB0121, KWB018, KWB013, KWB0151, KWB015, KWB020, KWB014Model KWB011, KWB012, KWB013, KWB014, KWB015, KWB016, KWB018, KWB020, KWB0111, KWB0121, KWB0151, KWB0171, KWB0172, KWB0181, KWB0191

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69542183QH006MK Basic UDI-DIDate23 Jan 2025RegisteredStatusActive

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  • Withdrawn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
KWB011, KWB012, KWB013, KWB014, KWB015, KWB016, KWB018, KWB020, KWB0111, KWB0121, KWB0151, KWB0171, KWB0172, KWB0181, KWB0191
Primary DI / UDI-DI
06954218304020, 06954218304112, 06954218304129, 06954218304082, 06954218304327, 06954218304044, 06954218304099, 06954218304303, 06954218304068, 06954218304051
Basic UDI-DI
69542183QH006MK
EMDN Code
T030301 Air flow blankets
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