Skip to content

MiniCollect® Complete 0.25 ml FX Sodium Fluoride / Potassium Oxalate grey cap, G-barcode label, pre-assembled with Carri

by Greiner Bio-One GmbH

Ref 480549Model MiniCollect® FX Sodium Fluoride / Potassium Oxalate 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, 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 Number912001757G0000056A2 Basic UDI-DI 19120049208095UDI-DIDate5 Aug 2026RegisteredStatusActive

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  • Withdrawn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
MiniCollect® FX Sodium Fluoride / Potassium Oxalate TUBE
Model / Reference
MiniCollect® FX Sodium Fluoride / Potassium Oxalate TUBE, 480549
Primary DI / UDI-DI
19120049208095
Basic UDI-DI
912001757G0000056A2
EMDN Code
W0501010203 Blood collection, capillary tubes
Device Class
Class A
EU market of registration
Austria

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