Skip to content

Kessler-Gelactif

by Ningbo Chinmed Technology Co., Ltd

Ref KW.H01Model FL-CB, FL-YB&FL-CB

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 Number697286436CT52 Basic UDI-DI 06972864362690UDI-DIDate28 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  • Withdrawn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
Hydrocolloid Dressing
Hydrocolloid blister plaster
Model / Reference
FL-CB, KW.H01, FL-YB&FL-CB
Primary DI / UDI-DI
06972864362690
Basic UDI-DI
697286436CT52, 697286436100004L
EMDN Code
M04040301 Hydrocolloid dressings, non-combined
Device Class
Class IIa
EU market of registration
Greece
Cyprus

Manufacturer details

EUDAMED SRN
CN-MF-000023983
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Ningbo Chinmed Technology Co., Ltd.

See all devices from Ningbo Chinmed Technology Co., Ltd. →

Properties

  • Sterile

Other properties (12)

  • 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