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Drive 15033BV-PKG-1-T

by Drive Devilbiss Healthcare

Drive 15033BV-PKG-1-T is a Class II device made by Drive Devilbiss Healthcare, listed in FDA GUDID since 16 Sep 2016 (UDI-DI 00822383211794), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00822383211794 UDI-DI Date16 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  • Withdrawn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
Drive
Generic name
Electrical assistive bed
Model / reference
15033BV-PKG-1-T
Primary DI / UDI-DI
00822383211794
FDA product code
FNL
GMDN term
Electrical assistive bed
Device class
Class II
Regulation number
880.5100
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FNL (BED, AC-POWERED ADJUSTABLE HOSPITAL).

Other devices from Drive Devilbiss Healthcare

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Properties

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