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Device Explorer · FDA GUDID · GMDN 34927

Patient lifting system amputee sling

A lifting device used together with a patient lifting system to provide a support for an amputee that is being lifted in a sitting position with their body (back, arms, and buttocks) enveloped within the sling. It is typically designed as a U-shaped piece of s

US‑registered devices67in 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

Arjohuntleigh Ab3857%
Handi-Move1827%
Etac A/S69%
Liko Ab57%

Top labelers

CompanyDevicesShare
Arjohuntleigh Ab3857%
Handi-Move1827%
Etac A/S69%
Liko Ab57%

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

Brand names on the register (sample)

MoliftHandi-Move SlingArjo SlingLiko Amputee HighBack Sling™, Mod. 75

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-Powered38
FSALift, patient, non-ac-powered23
IKXAID, TRANSFER6

GMDN & GCC registration

  • GMDN code 34927 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 0% · OTC 57%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

No structured size data on the register.

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

How many patient lifting system amputee sling products are registered in the US?

67 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Patient lifting system amputee sling", from 4 companies. The largest labeler is Arjohuntleigh Ab with 57% of records.

Which FDA product codes apply?

FSA (Lift, Patient, Non-Ac-Powered), FSA (Lift, patient, non-ac-powered), IKX (AID, TRANSFER)

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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