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Device Explorer · FDA GUDID · GMDN 40538

Manual patient lifting belt/harness

A device used to assist healthcare professionals or attending persons to physically move and lift a patient or a person with a disability (e.g., from the floor to a bed). The device is typically made strong textile materials (e.g., nylon or canvas) consisting

US‑registered devices72in commercial distribution
Companies14labelers on GUDID
Single‑use7%of device records
Sterile0%labelled sterile
Prescription0%Rx‑only share
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Share of device records

We Stitch Stuff, Llc1622%
Synchronis Medical, Llc1521%
Medi Care System Slu912%
Etac Immedia A/S811%
Ningbo Tealmed Emergency Products Co., Ltd.46%
Liko Ab46%
Hovertech International46%
Twin Med, Llc46%

Top labelers

CompanyDevicesShare
We Stitch Stuff, Llc1622%
Synchronis Medical, Llc1521%
Medi Care System Slu912%
Etac Immedia A/S811%
Ningbo Tealmed Emergency Products Co., Ltd.46%
Liko Ab46%
Hovertech International46%
Twin Med, Llc46%
Handi-Move23%
Merits Health Products Co., Ltd.23%
Silvalea Limited11%
Djo, Llc11%

Company = labeler of record on GUDID. 14 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

TealmedImmediaHandi-Move SlideBirthing Sling ManualMERITSPROCAREHandyBelt™Binder LifteasycareHoverJackEvacuation HoverJackViveHydraulic Patient LiftProCureMobi-toolsMobi-tools Grip

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

FDA product codes

CodeNameDevices
IKXAid, Transfer36
IKXAID, TRANSFER12
FMRDEVICE, TRANSFER, PATIENT, MANUAL11
FNGLIFT, PATIENT, AC-POWERED5
IQBBelt, Wheelchair4
FSALift, Patient, Non-Ac-Powered3

GMDN & GCC registration

  • GMDN code 40538 · non‑implantable
  • Single‑use 7% · sterile 0% · Rx‑only 0% · OTC 29%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Width (Inch) · 9Length (Inch) · 4

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

How many manual patient lifting belt/harness products are registered in the US?

72 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Manual patient lifting belt/harness", from 14 companies. The largest labeler is We Stitch Stuff, Llc with 22% of records.

Which FDA product codes apply?

IKX (Aid, Transfer), IKX (AID, TRANSFER), FMR (DEVICE, TRANSFER, PATIENT, MANUAL), 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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