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Disposable blood collection tubes

by Weihai Sunway Medical Technology Co., Ltd 10 variants

Ref Sodium Fluoride & EDTA 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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number697655656TUBE0178Z Basic UDI-DI 06976556562177UDI-DIDate29 Jan 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  • Withdrawn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
Sodium Fluoride & EDTA Tube
Primary DI / UDI-DI
06976556562177
Basic UDI-DI
697655656TUBE0178Z
EMDN Code
W050101010201 Blood collection, tubes with additives or serum separator
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

Other devices from Weihai Sunway Medical Technology Co., Ltd

See all devices from Weihai Sunway Medical Technology Co., Ltd →

Properties

  • Sterile
  • Near-Patient Testing

Other properties (9)

  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Professional Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No