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Blood Collection Tube

by Sanmen Minsheng Medical Appliances Co., Ltd.

Ref Plain TubeModel Plain Tube; Gel and Clot Activator Tube; Pro-coagulation Tube; PT Tube; EDTA Tube; Sodium Heparin Tube; Lithium Heparin Tube; ESR Tube; Glucose Tube

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 Number697941945CollectionTubeTY Basic UDI-DI 06979419450307UDI-DIDate29 Dec 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  • Withdrawn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
Blood Collection Tube
Model / Reference
Plain Tube, Gel and Clot Activator Tube, Pro-coagulation Tube, PT Tube, EDTA Tube, Sodium Heparin Tube, Lithium Heparin Tube, ESR Tube, Glucose Tube
Primary DI / UDI-DI
06979419450307
Basic UDI-DI
697941945CollectionTubeTY
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-000051043
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Sanmen Minsheng Medical Appliances 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