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Device Explorer · FDA GUDID · GMDN 40536

Patient lifting system stretcher

A lifting device used together with a patient lifting system to provide a support for an incapacitated patient or a person with a disability that is being lifted in a lying (horizontal) position for transfer and (re)positioning. It is designed as an elongated

US‑registered devices210in commercial distribution
Companies13labelers on GUDID
Single‑use3%of device records
Sterile0%labelled sterile
Prescription44%Rx‑only share
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Share of device records

Diacor, Inc.8038%
Arjohuntleigh Ab3316%
Lifeport, Llc2110%
Ez Way, Inc.199%
Liko Ab189%
Qfix136%
Silvalea Limited94%
Wuxi Emsrun Technology Co., Ltd.42%

Top labelers

CompanyDevicesShare
Diacor, Inc.8038%
Arjohuntleigh Ab3316%
Lifeport, Llc2110%
Ez Way, Inc.199%
Liko Ab189%
Qfix136%
Silvalea Limited94%
Wuxi Emsrun Technology Co., Ltd.42%
Etac A/S42%
Gbuk Group Limited31%
Jiangsu Rixin Medical Equipment Co.,Ltd21%
Handi-Move21%

Company = labeler of record on GUDID. 13 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

EMSRUNRED LEAFMoliftHandi-Move SlingGBUK LtdBananaAIRPALArjo SlingStretcher Sling Mesh Extra LargeStretcher Sling Mesh LargeStretcher Sling Mesh MediumStretcher Sling Mesh SmallIn-Situ Repositioning Sheet Extra LargeIn-Situ Repositioning Sheet LargeIn-Situ Repositioning Sheet MediumRepositioning Sheet Close Weave Polyester

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

FDA product codes

CodeNameDevices
FRZDevice, Patient Transfer, Powered80
FSALift, Patient, Non-Ac-Powered50
FMRDevice, Transfer, Patient, Manual26
FSALift, patient, non-ac-powered20
JAKSystem, x-ray, tomography, computed15
IYEAccelerator, linear, medical15

GMDN & GCC registration

  • GMDN code 40536 · non‑implantable
  • Single‑use 3% · sterile 0% · Rx‑only 44% · OTC 16%
  • 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 stretcher products are registered in the US?

210 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Patient lifting system stretcher", from 13 companies. The largest labeler is Diacor, Inc. with 38% of records.

Which FDA product codes apply?

FRZ (Device, Patient Transfer, Powered), FSA (Lift, Patient, Non-Ac-Powered), FMR (Device, Transfer, Patient, Manual), FSA (Lift, patient, non-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.

How do I get quotes?

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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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