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Probasics RLASXRBW

by Drive Devilbiss Healthcare

Probasics RLASXRBW is a Class I device made by Drive Devilbiss Healthcare, listed in FDA GUDID since 24 Jan 2024 (UDI-DI 00815067012688), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00815067012688 UDI-DI Date24 Jan 2024ListedStatusListed 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  • Withdrawn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
Probasics
Generic name
Handgrip disability-assistive walker, non-powered, foldable
Model / reference
RLASXRBW
Primary DI / UDI-DI
00815067012688
FDA product code
ITJ
GMDN term
Handgrip disability-assistive walker, non-powered, foldable
Device class
Class I
Regulation number
890.3825
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code ITJ (Walker, Mechanical).

Other devices from Drive Devilbiss Healthcare

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Properties

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