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IBA QUASAR™ Programmable Respiratory Motion Phantom 2 100-1026

by Modus Medical Devices Inc

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberG34310010260 UDI-DI Date17 Dec 2025ListedStatusListed 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  • Withdrawn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
IBA QUASAR™ Programmable Respiratory Motion Phantom 2
Generic Name
Multi-modality therapeutic radiation phantom, test object
Model / Ref / Catalog
100-1026
Primary DI / UDI-DI
G34310010260
FDA Product Code
LHO
GMDN Term
Multi-modality therapeutic radiation phantom, test object
Device Class
Class I
Regulation Number
892.1940
GUDID distribution status
In Commercial Distribution

Other devices from Modus Medical Devices Inc

See all devices from Modus Medical Devices Inc →

Properties

  • Premarket Exempt

Other properties (13)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No