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V-Tube

by AB Medical, Inc. 97 variants

Ref 500903

Active European Union

CE IVDD

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-08809357964315 Basic UDI-DI 08809357964315UDI-DIDate12 Oct 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  • Withdrawn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/IVDD Active

Specification

EUDAMED

Device Name
EDTA K2 9.0ml 1200pcs
Model / Reference
500903
Primary DI / UDI-DI
08809357964315
Basic UDI-DI
B-08809357964315
EMDN Code
W050101010201 Blood collection, tubes with additives or serum separator
Device Class
Class IVD General
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
KR-MF-000026779
Authorised representative
KTR Europe GmbH DE-AR-000005685

Other devices from AB Medical, Inc.

See all devices from AB Medical, Inc. →

Properties

  • Sterile

Other properties (9)

  • 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