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Non Vacuum Blood Collection Tube

by Cangzhou Fukang Medical Supplies Co., Ltd 5 variants

Ref Sodium Fluoride (Heparin) Tube, EDTAK2, EDTAK3, Sodium Citrate 1:4 Tube, Sodium Fluoride (Sodium Oxalate) Tube, Lithium Heparin Tube, Gel + Clot Activator Tube, Clot Activator Tube, EDTANa2Model Plain Tube Clot Activator Tube Sodium Heparin Tube Lithium Heparin Tube EDTAK2 EDTAK3 EDTANa2 Sodium Citrate1:9 Tube 1:4 Sodium Citrate1:4 Tube （EDTA）Sodium Fluoride （EDTA） Tube Sodium Fluoride (Sodium Oxalate) Tube, Plain Tube,Clot Activator Tube,Sodium Heparin Tube,Lithium Heparin Tube,EDTAK2,EDTAK3,EDTANa2,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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number697555099cxgf0049D Basic UDI-DI Date30 Jan 2023RegisteredStatusActive

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  • Withdrawn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
Non Vacuum Blood Collection Tube
Vacuum Blood Collection Tube
Model / Reference
Plain Tube Clot Activator Tube Sodium Heparin Tube Lithium Heparin Tube EDTAK2 EDTAK3 EDTANa2 Sodium Citrate1:9 Tube 1:4 Sodium Citrate1:4 Tube （EDTA）Sodium Fluoride （EDTA） Tube Sodium Fluoride (Sodium Oxalate) Tube, Sodium Fluoride (Heparin) Tube, EDTAK2, EDTAK3, Plain Tube, Clot Activator Tube, Sodium Heparin Tube, Lithium Heparin Tube, EDTANa2, etc., Sodium Citrate 1:4 Tube, Sodium Fluoride (Sodium Oxalate) Tube, Gel + Clot Activator Tube
Primary DI / UDI-DI
06975550990153, 06975550990085, 06975550990092, 06975550990252, 06975550990122, 06975550990146, 06975550990078, 06975550990160, 06975550990054, 06975550990108, 06975550990290
Basic UDI-DI
697555099cxgf0049D, 697555099cxg003JY
EMDN Code
W050101010202, W050101010101
Device Class
Class A
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000027309
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Cangzhou Fukang Medical Supplies Co., Ltd

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Properties

  • Reagent
  • Near-Patient Testing
  • Professional Testing
  • Companion Diagnostics

Other properties (7)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Surgical Instrument: No
  • New Device: No