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Visionix VX110

by Luneau Technology Operations

Ref VX110

Visionix VX110 is a device classified as Class IIa in the EU and Class I in the US made by Luneau Technology Operations, registered in EUDAMED on 7 May 2026 (Basic UDI-DI 13664188000060LE) and listed in FDA GUDID since 8 Jun 2023 (UDI-DI 03664188000060), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number13664188000060LE Basic UDI-DI 03664188000060UDI-DIDate7 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number03664188000060 UDI-DI Date8 Jun 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 13664188000060LE registered 7 May 2026 Active
  • FDA GUDID UDI-DI 03664188000060 listed 8 Jun 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 03664188000060
  2. Registered EUDAMED 13664188000060LE

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
VX110 EUDAMED
Visionix GUDID
Generic name
Automated ophthalmic refractometer
Model / reference
VX110
Primary DI / UDI-DI
03664188000060
Basic UDI-DI
13664188000060LE
FDA product code
HKO, MXK
EMDN code
Q0299 Ophthalmic devices - other
GMDN term
Automated ophthalmic refractometer
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
886.1760, 886.1850
EU registration type
Standard device
EU market of registration
France
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class I

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Automated ophthalmic refractometerPupillometer, electrically-powered

Similar devices in this category

Other devices filed under OPHTHALMIC DEVICES - OTHER.

Other devices from Luneau Technology Operations

See all devices from Luneau Technology Operations →

Properties

  • Measuring function
  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (21, all answered No)