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Melbourne Rapid Fields

by Glance Optical Pty Ltd

Ref MRF2.49Model Melbourne Rapid Fields Web

Active European Union

CE MDR

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/MDR Number++G583MRFONLINEEU2VJ Basic UDI-DI G583MRF249EU1UDI-DIDate14 Oct 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Model / Reference
Melbourne Rapid Fields Web, MRF2.49
Primary DI / UDI-DI
G583MRF249EU1
Basic UDI-DI
++G583MRFONLINEEU2VJ
EMDN Code
Z1212012092 Instruments for the assessment of visual functionality - medical device software
Device Class
Class I
Special Device Type
Software
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
AU-MF-000045585
Authorised representative
Donawa Lifescience Consulting Srl IT-AR-000007785

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No