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FlexStep V2

by Liftup A/S 64 variants

FlexStep V2 (103865) is an assistive passenger lift (FDA Class II; FDA product code PCE, Permanently Mounted Wheelchair Platform Lift) made by Liftup A/S, listed in FDA GUDID since 3 Jun 2021 (UDI-DI 05714420038653), 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 Number05714420038653 UDI-DI Date3 Jun 2021ListedStatusListed 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  • Withdrawn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
FlexStep
Generic name
Assistive passenger lift
Model / Ref / Catalog
FlexStep V2, 103865
Primary DI / UDI-DI
05714420038653
FDA product code
PCE
GMDN term
Assistive passenger lift
Device class
Class II
Regulation number
890.3930
GUDID distribution status
In Commercial Distribution

Related devices

Category: Assistive passenger lift

Similar devices

Also classified as Assistive passenger lift.

Other devices from Liftup A/S

See all devices from Liftup A/S →

Properties

  • Over-the-counter
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)