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Drive 13026KIT

by Drive Devilbiss Healthcare

Drive 13026KIT is a Class I device made by Drive Devilbiss Healthcare, listed in FDA GUDID since 21 Jun 2019 (UDI-DI 00822383178585), 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 Number00822383178585 UDI-DI Date21 Jun 2019ListedStatusListed 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  • Withdrawn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
Commode, manual
Model / reference
13026KIT
Primary DI / UDI-DI
00822383178585
FDA product code
FSA
GMDN term
Commode, manual
Device class
Class I
Regulation number
880.5510
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FSA (LIFT, PATIENT, NON-AC-POWERED).

Other devices from Drive Devilbiss Healthcare

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Properties

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