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DRX - Ascend System

by Carestream Health, Inc. 5 variants

DRX - Ascend System (1025907) is a X-ray system computer (FDA Class I; FDA product code LMD, System, digital image communications, radiological) made by Carestream Health, Inc., listed in FDA GUDID since 19 Jul 2017 (UDI-DI 60889974005226), 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 Number60889974005226 UDI-DI Date19 Jul 2017ListedStatusListed 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  • Withdrawn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 system computer, diagnostic, general-purpose
Model / Ref / Catalog
DRX - Ascend System, 1025907
Primary DI / UDI-DI
60889974005226
FDA product code
LMD
GMDN term
X-ray system computer, diagnostic, general-purpose
Device class
Class I
Regulation number
892.2020
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LMD (System, digital image communications, radiological).

Other devices from Carestream Health, Inc.

See all devices from Carestream Health, Inc. →

Properties

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