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Brainomix 360 e-CTA 11.3

by Brainomix Limited

Brainomix 360 e-CTA 11.3 is a Class II device made by Brainomix Limited, listed in FDA GUDID since 20 Mar 2025 (UDI-DI B720BX360ECTA1130), 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 NumberB720BX360ECTA1130 UDI-DI Date20 Mar 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  • Withdrawn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
Brainomix 360 e-CTA
Generic name
X-ray image interpretive software
Model / reference
11.3
Primary DI / UDI-DI
B720BX360ECTA1130
FDA product code
LLZ, QIH
GMDN term
X-ray image interpretive software
Device class
Class II
Regulation number
892.2050
GUDID distribution status
In Commercial Distribution

Related devices

Category: X-ray image interpretive software

Similar devices

Other devices filed under FDA product code LLZ (System, Image Processing, Radiological).

Other devices from Brainomix Limited

See all devices from Brainomix Limited →

Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)