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Disposable swabs

by Cangzhou Lankang Medical Instruments Developing Co., Ltd. 26 variants

Ref LK-210A

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 Number697235535078KJ Basic UDI-DI 06972355350786UDI-DIDate18 Mar 2024RegisteredStatusActive

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  • Withdrawn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

Model / Reference
LK-210A
Primary DI / UDI-DI
06972355350786
Basic UDI-DI
697235535078KJ
EMDN Code
Q019006 Dental material application tips and brushes, single-use
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
CN-MF-000002346
Authorised representative
Lotus NL B.V. NL-AR-000000121

Other devices from Cangzhou Lankang Medical Instruments Developing Co., Ltd.

See all devices from Cangzhou Lankang Medical Instruments Developing 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