Skip to content

MI Product Line 061323

by Medical Illumination International, Inc

MI Product Line 061323 is a mobile examination/treatment room light (FDA Class I; FDA product code KZF, Device, Medical Examination, Ac Powered) made by Medical Illumination International, Inc, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 00816835020225), 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 Number00816835020225 UDI-DI Date23 Sep 2016ListedStatusListed 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  • Withdrawn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
MI Product Line
Generic name
Mobile examination/treatment room light
Model / reference
061323
Primary DI / UDI-DI
00816835020225
FDA product code
KZF
GMDN term
Mobile examination/treatment room light
Device class
Class I
Regulation number
880.6320
GUDID distribution status
In Commercial Distribution

Related devices

Category: Mobile examination/treatment room light

Similar devices in this category

Other devices filed under Mobile examination/treatment room light.

Other devices from Medical Illumination International, Inc

See all devices from Medical Illumination International, Inc →

Properties

  • Premarket exempt
  • Serial number
Other properties (13, all answered No)