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Vacuum Blood Collection Tube

by Zhejiang Kangshi Medical Devices Co., Ltd 15 variants

Ref KS-Z (13x75mm; 13x100mm; 16x100mm; 12x60mm; 8x120mm; PET; PP; GLASS)Model KS-Z (13x75mm; 13x100mm; 16x100mm; 12x60mm; 8x120mm; PET; PP; GLASS), KS-CN (13x75mm; 13x100mm; 16x100mm; 12x60mm; 8x120mm; PET; PP; GLASS), etc

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 Number69490661VBCT001X4 Basic UDI-DI 06949066100009UDI-DIDate24 Jun 2025RegisteredStatusActive

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  • Withdrawn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
Vacuum Blood Collection Tube
Model / Reference
KS-Z (13x75mm, 13x100mm, 16x100mm, 12x60mm, 8x120mm, PET, PP, GLASS), KS-CN (13x75mm, etc
Primary DI / UDI-DI
06949066100009
Basic UDI-DI
69490661VBCT001X4
EMDN Code
W050101010201 Blood collection, tubes with additives or serum separator
Device Class
Class A
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000047239
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Zhejiang Kangshi Medical Devices Co., Ltd

See all devices from Zhejiang Kangshi Medical Devices Co., Ltd →

Properties

  • Professional Testing

Other properties (10)

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