Skip to content

Water Bath AWB210

by Amos Scientific Pty., Ltd

Ref AWB210

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 Number9309001291143XJ Basic UDI-DI 09309001291143UDI-DIDate8 Jul 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  • Withdrawn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

Model / Reference
AWB210
Primary DI / UDI-DI
09309001291143
Basic UDI-DI
9309001291143XJ
EMDN Code
W0202059011 Sample preparation units for chromosomic analysis
Device Class
Class A
EU market of registration
Romania

Manufacturer details

EUDAMED SRN
AU-MF-000036895
Authorised representative
Luxus Lebenswelt GmbH DE-AR-000005110

Other devices from Amos Scientific Pty., Ltd

See all devices from Amos Scientific Pty., Ltd →

Properties

  • Professional Testing
  • Surgical Instrument

Other properties (9)

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