Skip to content

Vitra

by Quantel Medical

Vitra is a Class II device made by Quantel Medical, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 03700542625132), registry data as of 21 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 21 Oct 2026.

Regulatory status

as of registry sync 21 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number03700542625132 UDI-DI Date23 Sep 2016ListedStatusListed 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  • Withdrawn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

Generic name
Ophthalmic solid-state laser system
Model / reference
VITRA
Description
Ophthalmic Laser Photocoagulator 532nm MonoSpot Laser Retinal Photocoagulation
Primary DI / UDI-DI
03700542625132
FDA product code
HQF
GMDN term
Ophthalmic solid-state laser system
Device class
Class II
Regulation number
886.4390
GUDID distribution status
In Commercial Distribution

Related devices

Category: Ophthalmic solid-state laser system

Similar devices in this category

Other devices filed under Ophthalmic solid-state laser system.

Other devices from Quantel Medical

See all devices from Quantel Medical →

Properties

  • Serial number
Other properties (14, all answered No)