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Device Explorer · FDA GUDID · GMDN 45386

Stand-up mobile patient lifting system, manual

A non-powered, mobile assembly of devices designed to enable one person to lift an incapacitated patient or a person with a disability from a sitting position into a standing position and then move them from one place to another by physically pushing it with m

US‑registered devices58in commercial distribution
Companies4labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription0%Rx‑only share
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Share of device records

Vancare Inc4883%
Handicare Usa, Inc.610%
1073849 Ontario Limited23%
Gf Health Products, Inc.23%

Top labelers

CompanyDevicesShare
Vancare Inc4883%
Handicare Usa, Inc.610%
1073849 Ontario Limited23%
Gf Health Products, Inc.23%

Company = labeler of record on GUDID. 4 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

WECAREVancare Vera LiftUltramove - TollosHandicareLumex

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
FSALift, Patient, Non-Ac-Powered56
FNGLift, Patient, Ac-Powered2

GMDN & GCC registration

  • GMDN code 45386 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 0% · OTC 3%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Height (Inch) · 2Width (Inch) · 2Depth (Inch) · 2

Use these as the dimensions to specify in a tender line.

How many stand-up mobile patient lifting system, manual products are registered in the US?

58 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Stand-up mobile patient lifting system, manual", from 4 companies. The largest labeler is Vancare Inc with 83% of records.

Which FDA product codes apply?

FSA (Lift, Patient, Non-Ac-Powered), FNG (Lift, Patient, Ac-Powered)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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