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Colposcope System

by Xuzhou Kernel Medical Equipment Co., Ltd.

Ref 06928798621068Model KN-2200、KN-2200A、KN-2200Ⅰ、KN-2200B、KN-2200BⅠ、KN-2200Ⅰ(H)

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number692879862203E Basic UDI-DI 06928798621068UDI-DIDate9 Mar 2023RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
KN-2200、KN-2200A、KN-2200Ⅰ、KN-2200B、KN-2200BⅠ、KN-2200Ⅰ(H), 06928798621068
Primary DI / UDI-DI
06928798621068
Basic UDI-DI
692879862203E
Direct Marketing DI
06928798621068
EMDN Code
Z12020703 Colposcopes
Device Class
Class I
EU market of registration
Hungary

Manufacturer details

EUDAMED SRN
CN-MF-000020694
Authorised representative
Caretechion GmbH DE-AR-000005946

Other devices from Xuzhou Kernel Medical Equipment Co., Ltd.

See all devices from Xuzhou Kernel Medical Equipment Co., Ltd. →

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