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Non Vacuum Blood Collection Tube

by Shandong Chengwu Medical Products Factory 49 variants

Ref Sodium Fluoride 13*75mm 5mlModel No Additive, Clot Activator, Gel & Clot Activator, Sodium Citrate (1:4), Sodium Citrate (1:9), Sodium/Lithium Heparin, EDTA K2/K3, Sodium Fluoride

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number697390596NVBCT018P Basic UDI-DI 06973905960684UDI-DIDate28 Jul 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  • Withdrawn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
Model / Reference
No Additive, Clot Activator, Gel & Clot Activator, Sodium Citrate (1:4), Sodium Citrate (1:9), Sodium/Lithium Heparin, EDTA K2/K3, Sodium Fluoride, Sodium Fluoride 13*75mm 5ml
Primary DI / UDI-DI
06973905960684
Basic UDI-DI
697390596NVBCT018P
EMDN Code
W050101010201 Blood collection, tubes with additives or serum separator
Device Class
Class A
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CN-MF-000003370
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

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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