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Table RAD DST 10273252

by Siemens Healthcare GmbH

Table RAD DST 10273252 is a Class II device made by Siemens Healthcare GmbH, listed in FDA GUDID since 2 Feb 2017 (UDI-DI 04056869009889), registry data as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04056869009889 UDI-DI Date2 Feb 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  • Withdrawn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

Trade name
Table RAD DST
Generic name
Basic diagnostic x-ray system table, powered
Model / reference
10273252
Primary DI / UDI-DI
04056869009889
FDA product code
KXJ
GMDN term
Basic diagnostic x-ray system table, powered
Device class
Class II
Regulation number
892.1980
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KXJ (Table, radiologic).

Other devices from Siemens Healthcare GmbH

See all devices from Siemens Healthcare GmbH →

Properties

  • Prescription use
  • Premarket exempt
  • Serial number
Other properties (12, all answered No)