Skip to content

VISIUSmatrix Application Platform 4.0 KIT

by IMRIS Imaging, Inc.

VISIUSmatrix Application Platform 4.0 KIT is a Class I device made by IMRIS Imaging, Inc., listed in FDA GUDID since 15 Sep 2020 (UDI-DI 00857534006646), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00857534006646 UDI-DI Date15 Sep 2020ListedStatusListed 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  • Withdrawn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 application software
Model / reference
Application Platform 4.0 KIT
Primary DI / UDI-DI
00857534006646
FDA product code
LMD
GMDN term
Operating room audiovisual data/device management system application software
Device class
Class I
Regulation number
892.2020
GUDID distribution status
In Commercial Distribution

Related devices

Category: Operating room audiovisual data/device management systemOperating room audiovisual data/device management system application software

Similar devices

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

Other devices from IMRIS Imaging, Inc.

See all devices from IMRIS Imaging, Inc. →

Properties

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