Skip to content

ORT200 Table

by IMRIS Imaging, Inc.

ORT200 Table is a Class II device made by IMRIS Imaging, Inc., listed in FDA GUDID since 31 Mar 2017 (UDI-DI 00857534006479), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00857534006479 UDI-DI Date31 Mar 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  • Withdrawn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
Basic diagnostic x-ray system table, powered
Model / reference
ORT200
Primary DI / UDI-DI
00857534006479
FDA product code
KXJ, FQO
GMDN term
Basic diagnostic x-ray system table, powered
Device class
Class II
Regulation number
892.1980, 878.4960
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Similar devices

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

Other devices from IMRIS Imaging, Inc.

See all devices from IMRIS Imaging, Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)