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UniRay DF930002

by Uniray Medical LLP

UniRay DF930002 is a Class I device made by Uniray Medical LLP, listed in FDA GUDID since 18 Feb 2023 (UDI-DI 08904333252551), 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 Number08904333252551 UDI-DI Date18 Feb 2023ListedStatusListed 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  • Withdrawn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
UniRay
Generic name
Digital imaging storage phosphor screen
Model / reference
DF930002
Primary DI / UDI-DI
08904333252551
FDA product code
LMB
GMDN term
Digital imaging storage phosphor screen
Device class
Class I
Regulation number
892.2010
GUDID distribution status
In Commercial Distribution

Related devices

Category: Digital imaging storage phosphor screen

Similar devices

Other devices filed under FDA product code LMB (Device, Digital Image Storage, Radiological).

Other devices from Uniray Medical LLP

See all devices from Uniray Medical LLP →

Properties

  • Over-the-counter
  • Premarket exempt
  • Manufacturing date
Other properties (12, all answered No)