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Qg-50-2

by Carestream Health, Inc. 3 variants

Qg-50-2 (1016393) is a Class I device made by Carestream Health, Inc., listed in FDA GUDID since 16 Sep 2016 (UDI-DI 60889974000511), registry data as of 8 Jun 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 8 Jun 2026.

Regulatory status

as of registry sync 8 Jun 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number60889974000511 UDI-DI Date16 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  • Withdrawn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
Diagnostic x-ray system generator, stationary
Model / Ref / Catalog
QG-50-2, 1016393
Primary DI / UDI-DI
60889974000511
FDA product code
IZO
GMDN term
Diagnostic x-ray system generator, stationary
Device class
Class I
Regulation number
892.1700
GUDID distribution status
In Commercial Distribution

Related devices

Category: Diagnostic x-ray system generator, stationary

Similar devices in this category

Other devices filed under Diagnostic x-ray system generator, stationary.

Other devices from Carestream Health, Inc.

See all devices from Carestream Health, Inc. →

Properties

  • Premarket exempt
  • Serial number
Other properties (13, all answered No)