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VACUETTE® TUBE 3.5 ml LH Lithium Heparin Separator 13x75 green cap-yellow ring, non-ridged

by Greiner Bio-One GmbH 2 variants

Ref 454008AModel VACUETTE® TUBE LH Lithium Heparin Separator

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-19120126130011 Basic UDI-DI 19120126130011UDI-DIDate20 Aug 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  • Withdrawn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
VACUETTE® TUBE LH Lithium Heparin Separator
Model / Reference
VACUETTE® TUBE LH Lithium Heparin Separator, 454008A
Primary DI / UDI-DI
19120126130011
Basic UDI-DI
B-19120126130011
EMDN Code
W050101010201 Blood collection, tubes with additives or serum separator
Device Class
Class IVD General
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
AT-MF-000024608

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See all devices from Greiner Bio-One GmbH →

Properties

  • Sterile
  • Animal Tissues
  • Professional Testing

Other properties (8)

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