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VISIUSmatrix 120906-000

by IMRIS Imaging, Inc.

VISIUSmatrix 120906-000 is a Class I device made by IMRIS Imaging, Inc., listed in FDA GUDID since 16 Oct 2026 (UDI-DI 00850085914026), registry data as of 2 Nov 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 2 Nov 2026.

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850085914026 UDI-DI Date16 Oct 2026ListedStatusListed 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  • Withdrawn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
VISIUSmatrix
Generic name
Operating room audiovisual data/device management system
Model / reference
120906-000
Primary DI / UDI-DI
00850085914026
FDA product code
LMD
GMDN term
Operating room audiovisual data/device management system
Device class
Class I
Regulation number
892.2020
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LMD (System, Digital Image Communications, Radiological).

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Properties

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