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Light Source Adaptor

by VitreQ B.V. 5 variants

Ref LF00.R02

Light Source Adaptor (LF00.R02) is a Class I device made by Vitreq B.V., registered in EUDAMED on 14 Feb 2023 (Basic UDI-DI 871921422989GX) and listed in FDA GUDID since 12 May 2019 (UDI-DI 08719214222307), active as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number871921422989GX Basic UDI-DI 08719214222307UDI-DIDate14 Feb 2023RegisteredStatusActive
United StatesGUDID listing GUDID Number08719214222307 UDI-DI Date12 May 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 871921422989GX registered 14 Feb 2023 Active
  • FDA GUDID UDI-DI 08719214222307 listed 12 May 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 08719214222307
  2. Registered EUDAMED 871921422989GX

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  • Withdrawn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
VitreQ
Generic name
Light source adaptor
Device name
Light Source Adaptor
Model / reference
LF00.R02
Primary DI / UDI-DI
08719214222307
Basic UDI-DI
871921422989GX
Direct marketing DI
18719214222304
FDA product code
FFY
EMDN code
Z12020480 Instruments for the acquisition and management of endoscopic and minimally invasive surgery images - hardware accessories
GMDN term
Light source adaptor
Device class
Class I
Regulation number
876.1500
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Manufacturer details

EUDAMED SRN
NL-MF-000000424

Similar devices in this category

Other devices filed under INSTRUMENTS FOR THE ACQUISITION AND MANAGEMENT OF ENDOSCOPIC AND MINIMALLY INVASIVE SURGERY IMAGES - HARDWARE ACCESSORIES.

Other devices from Vitreq B.V.

See all devices from Vitreq B.V. →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (21, all answered No)