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Inspired by Drive APP-4000L-DX

by Drive Devilbiss Healthcare

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00822383002323 UDI-DI Date20 Feb 2020ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Inspired by Drive
Generic Name
Freestanding patient positioner, reusable
Model / Reference
APP-4000L-DX
Primary DI / UDI-DI
00822383002323
FDA Product Code
PRN
GMDN Term
Freestanding patient positioner, reusable
Device Class
Class I
Regulation Number
880.5680
GUDID distribution status
In Commercial Distribution

Related devices

Category: Freestanding patient positioner, reusable

Other devices from Drive Devilbiss Healthcare

See all devices from Drive Devilbiss Healthcare →

Properties

  • Over-the-Counter
  • Premarket Exempt
  • Serial Number

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No
  • Manufacturing Date: No