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Pf PF2006-32

by Sunnex, Inc.

Pf PF2006-32 is a mobile examination/treatment room light (FDA Class I; FDA product code KZF, Device, medical examination, ac powered) made by Sunnex, Inc., listed in FDA GUDID since 26 Feb 2018 (UDI-DI 00853538008426), 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 Number00853538008426 UDI-DI Date26 Feb 2018ListedStatusListed 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  • Withdrawn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
Pf
Generic name
Mobile examination/treatment room light
Model / Ref / Catalog
PF2006-32
Primary DI / UDI-DI
00853538008426
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 Sunnex, Inc.

See all devices from Sunnex, Inc. →

Properties

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