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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 (mini rubber), Gel& Lithium Heparin Tube (mini rubber), Gel& Clot Activator Tube (mini lock), Gel& Sodium Heparin Tube, No Additive Tube (White), Gel& Lithium Heparin Tube (mini lock), Clot Activator Tube (mini lock), 3.2% Sodium Citrate Tubes, Sodium Fluoride& EDTA.K2 Tube (mini plastic), Sodium Heparin Tube (mini lock), Sodium Fluoride& Sodium Heparin Tube (mini lock), 3.2% Sodium Citrate Tube(0.109mol/L) (mini plastic), Clot Activator Tube (mini plastic), Gel& Lithium Heparin Tube (mini plastic), Clot Activator Tube（Orange）, No Additive Tube (mini plastic), Gel& EDTA.K2 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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number697655656TUBE01995 Basic UDI-DI Date29 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  • Withdrawn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
Model / Reference
No Additive Tube (mini rubber), QI-7.5.8-02, Gel& Lithium Heparin Tube (mini rubber), Gel& Clot Activator Tube (mini lock), Gel& Sodium Heparin Tube, No Additive Tube (White), Gel& Lithium Heparin Tube (mini lock), Clot Activator Tube (mini lock), 3.2% Sodium Citrate Tubes, Sodium Fluoride& EDTA.K2 Tube (mini plastic), Sodium Heparin Tube (mini lock), Sodium Fluoride& Sodium Heparin Tube (mini lock), 3.2% Sodium Citrate Tube(0.109mol/L) (mini plastic), Clot Activator Tube (mini plastic), Gel& Lithium Heparin Tube (mini plastic), Clot Activator Tube（Orange）, No Additive Tube (mini plastic), Gel& EDTA.K2 Tube
Primary DI / UDI-DI
06976556562191, 06976556562252, 06976556562412, 06976556562139, 06976556562566, 06976556562467, 06976556562399, 06976556562078, 06976556562382, 06976556562443, 06976556562474, 06976556562580, 06976556562283, 06976556562368, 06976556562559, 06976556562290, 06976556562054
Basic UDI-DI
697655656TUBE01995, 697655656TUBE0258Y, 697655656TUBE0418W, 697655656TUBE0138R, 697655656TUBE0569B, 697655656TUBE04698, 697655656TUBE0399B, 697655656TUBE0078W, 697655656TUBE03899, 697655656TUBE04494, 697655656TUBE0479A, 697655656TUBE0589F, 697655656TUBE02896, 697655656TUBE03695, 697655656TUBE05599, 697655656TUBE02998, 697655656TUBE0058S
EMDN Code
W050101010202, W050101010201
Device Class
Class A
EU market of registration
Poland

Manufacturer details

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

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Properties

  • Sterile
  • New Device

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