Skip to content

Vacuum Blood Collection Tube -Routine Blood Tubes-K2EDTA

by Suzhou CyrunFeh Medical Devices and Technology Co., Ltd. 5 variants

Ref 350530

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 Number6976093901002EDTA48 Basic UDI-DI Date2 Aug 2023RegisteredStatusActive

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  • Withdrawn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
Vacuum Blood Collection Tube -Routine Blood Tubes-K2EDTA
Model / Reference
350530
Primary DI / UDI-DI
16976093900026, 06976093900029
Basic UDI-DI
6976093901002EDTA48
EMDN Code
W050101010201 Blood collection, tubes with additives or serum separator
Device Class
Class A
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000034585
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Suzhou CyrunFeh Medical Devices and Technology Co., Ltd.

See all devices from Suzhou CyrunFeh Medical Devices and 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