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Disposable Vacuum Blood Collection Tubes

by Zhuhai Kanglilai Medical Equipment Co., Ltd

Model No Additive Tube（GAS）5mlΦ12.5×100mm No Additive Tube（PET）3mlΦ13×75mm No Additive Tube（GAS）4mlΦ13×75mm No Additive Tube（PET）4mlΦ13×75mm No Additive Tube（PET）1ml Φ13×75mm No Additive Tube（PET）2ml Φ13×75mm 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 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/IVDR Number697449799VBCT001B8 Basic UDI-DI 06974497991001UDI-DIDate20 Apr 2023RegisteredStatusActive

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  • Withdrawn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/IVDR Active

Specification

EUDAMED

Device Name
Disposable Vacuum Blood Collection Tubes
Model / Reference
No Additive Tube（GAS）5mlΦ12.5×100mm No Additive Tube（PET）3mlΦ13×75mm No Additive Tube（GAS）4mlΦ13×75mm No Additive Tube（PET）4mlΦ13×75mm No Additive Tube（PET）1ml Φ13×75mm No Additive Tube（PET）2ml Φ13×75mm etc
Primary DI / UDI-DI
06974497991001
Basic UDI-DI
697449799VBCT001B8
EMDN Code
W050101010201, W050101010202
Device Class
Class A
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000033320
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Properties

  • Sterile
  • Professional Testing

Other properties (9)

  • 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