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Drive Tr-A1601-Jb

by Drive Devilbiss Healthcare

Drive Tr-A1601-Jb is a Class I device made by Drive Devilbiss Healthcare, listed in FDA GUDID since 1 Feb 2020 (UDI-DI 00822383978895), 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 Number00822383978895 UDI-DI Date1 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  • Withdrawn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
Wheelchair/chair/stander headrest
Model / reference
TR-A1601-JB
Primary DI / UDI-DI
00822383978895
FDA product code
KNO
GMDN term
Wheelchair/chair/stander headrest
Device class
Class I
Regulation number
890.3910
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KNO (ACCESSORIES, WHEELCHAIR).

Other devices from Drive Devilbiss Healthcare

See all devices from Drive Devilbiss Healthcare →

Properties

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