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Vacuum Blood Collection Tube

by Yancheng Huida Medical Instruments Co., Ltd

Ref Plain tubeModel Plain tube; Clot activator tube; Sodium Citrate tube;ESR tube;Lithium Heparin tube; Sodium Heparin tube;Gel&Clot activator tube; Glucose tube; EDTA Tube(EDTA-K2/EDTA-K3/EDTA-Na2); PRP tube(ACD/ACD+ Gel 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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number697131752VBCT001PC Basic UDI-DI 06971317522414UDI-DIDate23 Jul 2026RegisteredStatusActive

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  • Withdrawn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
Plain tube, Clot activator tube, Sodium Citrate tube, ESR tube, Lithium Heparin tube, Sodium Heparin tube, Gel&Clot activator tube, Glucose tube, EDTA Tube(EDTA-K2/EDTA-K3/EDTA-Na2), PRP tube(ACD/ACD+ Gel etc.
Primary DI / UDI-DI
06971317522414
Basic UDI-DI
697131752VBCT001PC
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-000057276
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

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