Skip to content

Liver Phantom CCT288

by Providus Holdings, Inc.

Liver Phantom CCT288 is a Class I device made by Providus Holdings, Inc., listed in FDA GUDID since 9 Feb 2024 (UDI-DI 00812266030581), 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 Number00812266030581 UDI-DI Date9 Feb 2024ListedStatusListed 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  • Withdrawn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
Liver Phantom
Generic name
CT phantom, test object
Model / Ref / Catalog
CCT288
Primary DI / UDI-DI
00812266030581
FDA product code
IXF
GMDN term
CT phantom, test object
Device class
Class I
Regulation number
892.1940
GUDID distribution status
In Commercial Distribution

Related devices

Category: CT phantom, test object

Other devices from Providus Holdings, Inc.

See all devices from Providus Holdings, Inc. →

Properties

  • Single use
  • Premarket exempt
Other properties (13, all answered No)