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FoodPrint Accessories Sample Diluent

by Omega Diagnostics Ltd

Ref REBO-SDILGRT-10MLModel REBO-WBGRTV2-100ML and REBO-SDILGRT-10ML

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 Number506009393FOOPGPAD Basic UDI-DI 05060093930351UDI-DIDate15 May 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  • Withdrawn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
FoodPrint Reagent Accessories ( Wash Buffer and Sample Diluent)
Model / Reference
REBO-WBGRTV2-100ML and REBO-SDILGRT-10ML, REBO-SDILGRT-10ML
Primary DI / UDI-DI
05060093930351
Basic UDI-DI
506009393FOOPGPAD
EMDN Code
W0102010106 Immunoglobulin g subclass reagents
Device Class
Class A
EU market of registration
Ireland

Manufacturer details

EUDAMED SRN
GB-MF-000008490
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Omega Diagnostics Ltd

Properties

  • Reagent
  • Professional Testing

Other properties (9)

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