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Vacuum Blood Collection Tube

by Shandong Chengwu Huabo Medical Equipment Co., Ltd 225 variants

Ref Anticoagulant+Gel 8mlModel Clot Activator:1、2、3、4、5、6、7、8、9、10ml Plain Tube:1、2、3、4、5、6、7、8、9、10ml Heparin Sodium:1、2、3、4、5、6、7、8、9、10ml Lithium Heparin:1、2、3、4、5、6、7、8、9、10ml, 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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number697538735VBCTUP Basic UDI-DI 06975387351240UDI-DIDate17 Jun 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  • Withdrawn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
Clot Activator:1、2、3、4、5、6、7、8、9、10ml Plain Tube:1、2、3、4、5、6、7、8、9、10ml Heparin Sodium:1、2、3、4、5、6、7、8、9、10ml Lithium Heparin:1、2、3、4、5、6、7、8、9、10ml, etc, Anticoagulant+Gel 8ml
Primary DI / UDI-DI
06975387351240
Basic UDI-DI
697538735VBCTUP
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-000055916
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

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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