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Drive RTLPC23278

by Drive Devilbiss Healthcare

Drive RTLPC23278 is a Class I device made by Drive Devilbiss Healthcare, listed in FDA GUDID since 10 Jul 2017 (UDI-DI 00822383246178), 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 Number00822383246178 UDI-DI Date10 Jul 2017ListedStatusListed 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  • Withdrawn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
Elevation arm sling
Model / reference
RTLPC23278
Primary DI / UDI-DI
00822383246178
FDA product code
ILI
GMDN term
Elevation arm sling
Device class
Class I
Regulation number
890.3640
GUDID distribution status
In Commercial Distribution

Related devices

Category: Elevation arm sling

Other devices from Drive Devilbiss Healthcare

See all devices from Drive Devilbiss Healthcare →

Properties

  • Over-the-counter
  • Premarket exempt
Other properties (13, all answered No)