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Disposable Blood Collection Tubes

by Weihai Sunway Medical Technology Co., Ltd 10 variants

Ref QI-7.5.8-02Model No Additive Tube (Red), Gel& EDTA.K3 Tube (PURPLE), Gel& Clot Activator Tube (mini amber plastic), EDTA.K3 Tube (mini lock), EDTA.K2 Tube (mini plastic), EDTA.K2 Tube (mini lock), Gel& Lithium Heparin Tube, 3.8% Sodium Citrate Tube（0.129mol/L）, Sodium Fluoride& Sodium Heparin Tube (mini rubber), 3.2% Sodium Citrate Tube(0.109mol/L) (mini rubber), EDTA.K3 Tube (PINK), Lithium Heparin Tube (mini lock), Sodium Heparin Tube, EDTA.K2 Tube（pink）, Lithium Heparin Tube (mini rubber), Lithium Heparin Tube (mini plastic), Sodium Fluoride& EDTA.K2 Tube (mini lock), EDTA.K3 Tube (mini plastic), EDTA.K2 Tube (mini rubber), Sodium Heparin Tube (mini plastic), Clot activator tube (PINK), Double-wall Sodium Citrate Tube---3.8% Sodium Citrate(0.129mol/L), 3.8% sodium citrate tube（0.129mol/L）, Gel& Thrombin tube, No Activator Tube (mini lock), Gel& Clot Activator Tube (mini plastic), Sodium Heparin Tube (mini rubber), Gel& EDTA.K2 Tube (White ), Thrombin 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number697655656TUBE0028L Basic UDI-DI Date30 Jun 2026RegisteredStatusActive

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  • Withdrawn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 Blood Collection Tubes
Disposalble blood collection tubes
Model / Reference
No Additive Tube (Red), QI-7.5.8-02, Gel& EDTA.K3 Tube (PURPLE), Gel& Clot Activator Tube (mini amber plastic), EDTA.K3 Tube (mini lock), EDTA.K2 Tube (mini plastic), EDTA.K2 Tube (mini lock), Gel& Lithium Heparin Tube, 3.8% Sodium Citrate Tube（0.129mol/L）, Sodium Fluoride& Sodium Heparin Tube (mini rubber), 3.2% Sodium Citrate Tube(0.109mol/L) (mini rubber), EDTA.K3 Tube (PINK), Lithium Heparin Tube (mini lock), Sodium Heparin Tube, EDTA.K2 Tube（pink）, Lithium Heparin Tube (mini rubber), Lithium Heparin Tube (mini plastic), Sodium Fluoride& EDTA.K2 Tube (mini lock), EDTA.K3 Tube (mini plastic), EDTA.K2 Tube (mini rubber), Sodium Heparin Tube (mini plastic), Clot activator tube (PINK), Double-wall Sodium Citrate Tube---3.8% Sodium Citrate(0.129mol/L), Gel& Thrombin tube, No Activator Tube (mini lock), Gel& Clot Activator Tube (mini plastic), Sodium Heparin Tube (mini rubber), Gel& EDTA.K2 Tube (White ), Thrombin tube
Primary DI / UDI-DI
06976556562023, 06976556562528, 06976556562313, 06976556562436, 06976556562320, 06976556562429, 06976556562153, 06976556562115, 06976556562269, 06976556562573, 06976556562535, 06976556562450, 06976556562122, 06976556562511, 06976556562245, 06976556562351, 06976556562481, 06976556562337, 06976556562214, 06976556562344, 06976556562542, 06976556562108, 06976556562085, 06976556562504, 06976556562405, 06976556562306, 06976556562238, 06976556562597, 06976556562498
Basic UDI-DI
697655656TUBE0028L, 697655656TUBE05293, 697655656TUBE0318T, 697655656TUBE04392, 697655656TUBE0328V, 697655656TUBE0428Y, 697655656TUBE0158V, 697655656TUBE0118M, 697655656TUBE02692, 697655656TUBE0579D, 697655656TUBE05395, 697655656TUBE04596, 697655656TUBE0128P, 697655656TUBE0518Z, 697655656TUBE0248W, 697655656TUBE03593, 697655656TUBE0489C, 697655656TUBE0338X, 697655656TUBE0218Q, 697655656TUBE0348Z, 697655656TUBE05497, 697655656TUBE0108K, 697655656TUBE0088Y, 697655656TUBE0508X, 697655656TUBE0408U, 697655656TUBE0308R, 697655656TUBE0238U, 697655656TUBE0599H, 697655656TUBE0499E
EMDN Code
W050101010202, W050101010201
Device Class
Class A
EU market of registration
Poland
Cyprus
Italy

Manufacturer details

EUDAMED SRN
CN-MF-000025939
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Weihai Sunway Medical Technology Co., Ltd

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Properties

  • Sterile
  • New Device YesEUDAMEDNoEUDAMED

Other properties (9)

  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Professional Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No