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Micro Blood Collection Tube

by Zhejiang Gongdong Medical Technology Co., Ltd., 13 variants

Ref GD010SC, GD-EDTA.K2, GDC005SC8, GD005SFH, GD005A, GD-EDTA.K3, GDC005SFH, GDC005LHG, GDC005SH, GD005SGC, GD005LH, GDC010CA, GD005SH, GDC005SC, GD005CA, GDC010SC, GDC005CA, GDC010SPModel 3.2%Sodium citrate without capillary tube, EDTA.K2 capillary tube, 3.8%Sodium citrate with capillary tube, Micro Blood Collection Tube(Heparin sodium + Sodium Fluoride without capillary tube), Micro Blood Collection Tube(No addition without capillary tube), EDTA.K3 capillary tube, Micro Blood Collection Tube(Heparin sodium + Sodium Fluoride with capillary tube), Heparin Lithium+Gel with capillary tube, Micro Blood Collection Tube(Heparin sodium with capillary tube), Micro Blood Collection Tube(Gel+Clot activator without capillary tube), Micro Blood Collection Tube(Heparin lithium without capillary tube), Clot activator with capillary tube, Micro Blood Collection Tube(Heparin sodium without capillary tube), 3.2%Sodium citrate with capillary tube, Micro Blood Collection Tube(Clot activator without capillary tube), Sodium Flouride+Potassium Oxalate with capillary 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 Number6947462411111208LW Basic UDI-DI Date25 Oct 2025RegisteredStatusActive

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  • Withdrawn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

Model / Reference
3.2%Sodium citrate without capillary tube, GD010SC, EDTA.K2 capillary tube, GD-EDTA.K2, 3.8%Sodium citrate with capillary tube, GDC005SC8, Micro Blood Collection Tube(Heparin sodium + Sodium Fluoride without capillary tube), GD005SFH, Micro Blood Collection Tube(No addition without capillary tube), GD005A, EDTA.K3 capillary tube, GD-EDTA.K3, Micro Blood Collection Tube(Heparin sodium + Sodium Fluoride with capillary tube), GDC005SFH, Heparin Lithium+Gel with capillary tube, GDC005LHG, Micro Blood Collection Tube(Heparin sodium with capillary tube), GDC005SH, Micro Blood Collection Tube(Gel+Clot activator without capillary tube), GD005SGC, Micro Blood Collection Tube(Heparin lithium without capillary tube), GD005LH, Clot activator with capillary tube, GDC010CA, Micro Blood Collection Tube(Heparin sodium without capillary tube), GD005SH, 3.2%Sodium citrate with capillary tube, GDC005SC, Micro Blood Collection Tube(Clot activator without capillary tube), GD005CA, GDC010SC, GDC005CA, Sodium Flouride+Potassium Oxalate with capillary tube, GDC010SP
Primary DI / UDI-DI
06947462434292, 06947462436531, 06947462434988, 06947462430669, 06947462430614, 06947462436524, 06947462430591, 06947462421292, 06947462430584, 06947462430676, 06947462430645, 06947462430942, 06947462430652, 06947462421278, 06947462431468, 06947462430959, 06947462421261, 06947462430966
Basic UDI-DI
6947462411111208LW, 6947462411111212LM, 6947462411111209LY, 6947462411111189MK, 6947462411111184M9, 6947462411111211LK, 6947462411111182M5, 6947462411111177MC, 6947462411111181M3, 6947462411111190M4, 6947462411111187MF, 6947462411111203LL, 6947462411111188MH, 6947462411111201LG, 6947462411111185MB, 6947462411111202LJ
EMDN Code
W0501010203 Blood collection, capillary tubes
Device Class
Class A
EU market of registration
Romania
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000005694
Authorised representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Other devices from Zhejiang Gongdong Medical Technology Co., Ltd.

See all devices from Zhejiang Gongdong Medical Technology Co., Ltd. →

Properties

  • Sterile

Other properties (10)

  • 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
  • New Device: No