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Qt-Lch

by Carestream Health, Inc.

Qt-Lch (6573547) is a Class I device made by Carestream Health, Inc., listed in FDA GUDID since 16 Sep 2016 (UDI-DI 60889976573549), 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 Number60889976573549 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  • Withdrawn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
X-ray film cassette holder
Model / Ref / Catalog
QT-LCH, 6573547
Primary DI / UDI-DI
60889976573549
FDA product code
IXY
GMDN term
X-ray film cassette holder
Device class
Class I
Regulation number
892.1880
GUDID distribution status
In Commercial Distribution

Related devices

Category: X-ray film cassette holder

Similar devices in this category

Other devices filed under X-ray film cassette holder.

Other devices from Carestream Health, Inc.

See all devices from Carestream Health, Inc. →

Properties

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