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HexaMotion SDOS104-05

by Scandidos AB

HexaMotion SDOS104-05 is a multi-modality therapeutic radiation phantom (FDA Class I; FDA product code LHO, Instrument, Quality-Assurance, Radiologic) made by Scandidos AB, listed in FDA GUDID since 25 Sep 2016 (UDI-DI 17350005180055), 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 Number17350005180055 UDI-DI Date25 Sep 2016ListedStatusListed 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  • Withdrawn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
HexaMotion
Generic name
Multi-modality therapeutic radiation phantom, anthropomorphic
Model / Ref / Catalog
SDOS104-05
Primary DI / UDI-DI
17350005180055
FDA product code
LHO
GMDN term
Multi-modality therapeutic radiation phantom, anthropomorphic
Device class
Class I
Regulation number
892.1940
GUDID distribution status
In Commercial Distribution

Related devices

Category: Multi-modality therapeutic radiation phantom, anthropomorphic

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Properties

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