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IMAGE DIAGNOSTICS INC ISO-Drive

by Image Diagnostics, Inc. 4 variants

IMAGE DIAGNOSTICS INC ISO-Drive (A100-3225) is a Class II device made by Image Diagnostics, Inc., listed in FDA GUDID since 17 Feb 2022 (UDI-DI 00850977007706), 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 Number00850977007706 UDI-DI Date17 Feb 2022ListedStatusListed 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  • Withdrawn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
Image Diagnostics Inc
Generic name
Basic diagnostic x-ray system table, powered
Model / Ref / Catalog
ISO-Drive, A100-3225
Primary DI / UDI-DI
00850977007706
FDA product code
IXR
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 IXR (Table, Radiographic, Tilting).

Other devices from Image Diagnostics, Inc.

See all devices from Image Diagnostics, Inc. →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)