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Sun Nuclear MultiPHAN Phantom Kit 2823

by Sun Nuclear Corporation

Sun Nuclear MultiPHAN Phantom Kit 2823 is a Class I device made by Sun Nuclear Corporation, listed in FDA GUDID since 27 Aug 2021 (UDI-DI B13628230), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB13628230 UDI-DI Date27 Aug 2021ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Sun Nuclear MultiPHAN Phantom Kit
Generic name
CT phantom, test object
Model / reference
2823
Primary DI / UDI-DI
B13628230
FDA product code
LHO
GMDN term
CT phantom, test object
Device class
Class I
Regulation number
892.1940
GUDID distribution status
In Commercial Distribution

From the manufacturer

Manufacturer's product page: Sun Nuclear Patents

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Category: CT phantom, test object

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Properties

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