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Kessler-Primafix

by Ningbo Chinmed Technology Co., Ltd 17 variants

Ref KD.D02Model FT-TM & FT-FW & FT-XS

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 Number697286436200004X Basic UDI-DI 06972864362638UDI-DIDate25 Apr 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  • Withdrawn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
Wound Dressings
Model / Reference
FT-TM & FT-FW & FT-XS, KD.D02
Primary DI / UDI-DI
06972864362638
Basic UDI-DI
697286436200004X
EMDN Code
M04010101 Non-woven adhesive dressings, with absorbent pad
Device Class
Class IIa
EU market of registration
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