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Highlander II

by Harmar Summit, LLC 131 variants

Highlander II (VPL1000SRAACO) is a wheelchair/occupant lift (FDA Class II; FDA product code PCE, Permanently mounted wheelchair platform lift) made by Harmar Summit, LLC, listed in FDA GUDID since 22 Apr 2020 (UDI-DI 00817650024160), 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 Number00817650024160 UDI-DI Date22 Apr 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  • Withdrawn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
Highlander
Generic name
Wheelchair/occupant lift
Model / Ref / Catalog
Highlander II, VPL1000SRAACO
Primary DI / UDI-DI
00817650024160
FDA product code
PCE
GMDN term
Wheelchair/occupant lift
Device class
Class II
Regulation number
890.3930
GUDID distribution status
In Commercial Distribution

Related devices

Category: Wheelchair/occupant lift

Other devices from Harmar Summit, LLC

See all devices from Harmar Summit, LLC →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)