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icobrain mr 5.14

by icometrix NV

icobrain mr 5.14 is a medical device (FDA Class II; FDA product code LLZ, System, Image Processing, Radiological) made by icometrix NV, listed in FDA GUDID since 8 Dec 2023 (UDI-DI B621ICOBRAINMR5X14Y0), 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 NumberB621ICOBRAINMR5X14Y0 UDI-DI Date8 Dec 2023ListedStatusListed 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  • Withdrawn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
icobrain mr
Generic name
Radiology DICOM image processing application software
Model / reference
5.14
Primary DI / UDI-DI
B621ICOBRAINMR5X14Y0
FDA product code
LLZ
GMDN term
Radiology DICOM image processing application software
Device class
Class II
Regulation number
892.2050
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

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Properties

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