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Nexxis MNT-120

by Barco NV 3 variants

Nexxis MNT-120 (K9303082A) is a Class II device made by Barco NV, listed in FDA GUDID since 30 Jun 2016 (UDI-DI 05415334000827), not in commercial distribution (GUDID) as of 9 Nov 2026.

Listed FDA GUDID listing, not in commercial distribution

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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number05415334000827 UDI-DI Date30 Jun 2016ListedStatusListed GUDID: not 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  • Withdrawn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
Nexxis
Generic name
Operating room audiovisual data/device management system
Model / Ref / Catalog
MNT-120, K9303082A
Primary DI / UDI-DI
05415334000827
FDA product code
DXJ
GMDN term
Operating room audiovisual data/device management system
Device class
Class II
Regulation number
870.2450
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code DXJ (DISPLAY, CATHODE-RAY TUBE, MEDICAL).

Other devices from Barco NV

See all devices from Barco NV →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)