Skip to content

MiniCollect® TUBE 0.25/0.5 ml K3E K3EDTA lavender cap, G-barcode label

by Greiner Bio-One GmbH

Ref 480530Model MiniCollect® K3E K3EDTA TUBE

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE IVDR, withdrawn

Ended

Withdrawn

Date not published (CE IVDR)

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number912001757G00000449T Basic UDI-DI 19120049206930UDI-DIDate10 Aug 2026RegisteredStatusWithdrawn No longer placed on the EU market

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  • Withdrawn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European Union — CE/IVDR Withdrawn

Specification

EUDAMED

Device Name
MiniCollect® K3E K3EDTA TUBE
Model / Reference
MiniCollect® K3E K3EDTA TUBE, 480530
Primary DI / UDI-DI
19120049206930
Basic UDI-DI
912001757G00000449T
EMDN Code
W0501010203 Blood collection, capillary tubes
Device Class
Class A

Manufacturer details

EUDAMED SRN
AT-MF-000024608

Other devices from Greiner Bio-One GmbH

See all devices from Greiner Bio-One GmbH →

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