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Drive D574P-1070J

by Drive Devilbiss Healthcare

Drive D574P-1070J is a Class I device made by Drive Devilbiss Healthcare, listed in FDA GUDID since 11 Feb 2020 (UDI-DI 00822383157801), 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 Number00822383157801 UDI-DI Date11 Feb 2020ListedStatusListed 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  • Withdrawn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
Patient transfer sliding board
Model / reference
D574P-1070J
Description
Part Patient Room Parts Product Description Armrest,D574,Jade,1/ea
Primary DI / UDI-DI
00822383157801
FDA product code
KMN, INN
GMDN term
Patient transfer sliding board
Device class
Class I
Regulation number
880.6140, 890.3100
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code INN.

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Properties

  • Over-the-counter
  • Premarket exempt
  • Serial number
Other properties (12, all answered No)