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Disposable Vaccum Blood Collection Tube

by Shanghai Sunshore Medical Instruments Co., Ltd

Ref 13x75mm(1-5ml)Model 13x75mm(1-5ml),13x100mm(5-7ml),16x100mm(8-10ml);8x120mm Plain Tube,Pro-coagulation Tube ,Gel&Clot Activator Tube , EDTA Tube,PT Tube,ESR Tube, Heparin Tube, 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 Number698023123DVBCT001RY Basic UDI-DI 06980231236109UDI-DIDate6 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  • Withdrawn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
Disposable Vaccum Blood Collection Tube
Model / Reference
13x75mm(1-5ml), 13x100mm(5-7ml), 16x100mm(8-10ml), 8x120mm Plain Tube, Pro-coagulation Tube, Gel&Clot Activator Tube, EDTA Tube, PT Tube, ESR Tube, Heparin Tube, etc
Primary DI / UDI-DI
06980231236109
Basic UDI-DI
698023123DVBCT001RY
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-000056183
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