Skip to content

Qasar 500

by HTZ Limited

Ref 9925/001

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 Number5060242709925ST Basic UDI-DI 05060242700217UDI-DIDate24 Sep 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  • Withdrawn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
Beeline - QASAR 500SX
Model / Reference
9925/001
Primary DI / UDI-DI
05060242700217
Basic UDI-DI
5060242709925ST
EMDN Code
W02060199 Robotic sample processing systems - other
Device Class
Class A
EU market of registration
Hungary

Manufacturer details

EUDAMED SRN
UK-MF-000056273
Authorised representative
Advena Limited MT-AR-000000234

Properties

  • Human Tissues
  • Animal Tissues
  • Microbial Substances
  • Professional Testing
  • Surgical Instrument

Other properties (6)

  • Sterile: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • New Device: No