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Aodekang

by Cangzhou Fukang Medical Supplies Co., Ltd 3 variants

Model Inactivated Preserving Liquid, Non-inactivated Preserving Liquid

Active European Union

CE IVDR

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number697555099cyg002K9 Basic UDI-DI 06975550990023UDI-DIDate24 Aug 2022RegisteredStatusActive

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  • Withdrawn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/IVDR Active

Specification

EUDAMED

Device Name
Disposable Virus Sampling Tube
Model / Reference
Inactivated Preserving Liquid, Non-inactivated Preserving Liquid
Primary DI / UDI-DI
06975550990023
Basic UDI-DI
697555099cyg002K9
EMDN Code
W05019099 Samples collection devices - other
Device Class
Class A
EU market of registration
France

Manufacturer details

EUDAMED SRN
CN-MF-000027309
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Cangzhou Fukang Medical Supplies Co., Ltd

See all devices from Cangzhou Fukang Medical Supplies Co., Ltd →

Properties

  • Reagent
  • Professional Testing

Other properties (9)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No