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Drivemedical Trid-2A37-Linx

by Drive Devilbiss Healthcare

Listed FDA GUDID listing, not in commercial distribution

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 Number00822383967080 UDI-DI Date21 Jun 2019ListedStatusListed GUDID: not 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  • Withdrawn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
Drivemedical
Generic Name
Electric-motor-driven wheelchair, occupant-controlled
Model / Reference
TRID-2A37-LINX
Primary DI / UDI-DI
00822383967080
FDA Product Code
KNO
GMDN Term
Electric-motor-driven wheelchair, occupant-controlled
Device Class
Class I
Regulation Number
890.3910
GUDID distribution status
Not in Commercial Distribution

Other devices from Drive Devilbiss Healthcare

See all devices from Drive Devilbiss Healthcare →

Properties

  • Premarket Exempt
  • Serial Number

Other properties (12)

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