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VitreQ LF23.D01

by Vitreq B.V. 2 variants

VitreQ LF23.D01 is a Class II device made by Vitreq B.V., listed in FDA GUDID since 12 May 2019 (UDI-DI 08719214222109), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08719214222109 UDI-DI Date12 May 2019ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
VitreQ
Generic name
Ophthalmic fibreoptic light instrument, single-use
Model / reference
LF23.D01
Primary DI / UDI-DI
08719214222109
FDA product code
MPA
GMDN term
Ophthalmic fibreoptic light instrument, single-use
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ophthalmic fibreoptic light instrument, single-use

Similar devices in this category

Other devices filed under Ophthalmic fibreoptic light instrument, single-use.

Other devices from Vitreq B.V.

See all devices from Vitreq B.V. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)