Skip to content

MiniCollect® Complete 0.8 ml LH Lithium Heparin Separator light-green cap, pre-assembled with Carrier Tube 13x75, barcod

by Greiner Bio-One GmbH

Ref 480650Model MiniCollect® LH Lithium Heparin Sep 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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number912001757G0000048A3 Basic UDI-DI 19120049209344UDI-DIDate10 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  • Withdrawn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® LH Lithium Heparin Sep TUBE
Model / Reference
MiniCollect® LH Lithium Heparin Sep TUBE, 480650
Primary DI / UDI-DI
19120049209344
Basic UDI-DI
912001757G0000048A3
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

  • Animal Tissues
  • Professional Testing

Other properties (9)

  • Sterile: No
  • Human Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No