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Device Explorer · FDA GUDID · GMDN 37160

Patient transfer system, powered

A mains electricity (AC-powered) assembly of devices used to transfer a supine patient, typically from his/her bed or transport stretcher to an operating table or vice versa. It is usually installed in large operating room (OR) complexes and serves as a sluice

US‑registered devices111in commercial distribution
Companies9labelers on GUDID
Single‑use11%of device records
Sterile0%labelled sterile
Prescription6%Rx‑only share
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Share of device records

Hovertech International5953%
Air-Matt Incorporated2220%
Prestige Ameritech, Ltd.1312%
L I N E T Spol. S R.O.76%
Medline Industries, Inc.55%
Airpal, Inc.22%
Maquet Gmbh11%
Diacor, Inc.11%

Top labelers

CompanyDevicesShare
Hovertech International5953%
Air-Matt Incorporated2220%
Prestige Ameritech, Ltd.1312%
L I N E T Spol. S R.O.76%
Medline Industries, Inc.55%
Airpal, Inc.22%
Maquet Gmbh11%
Diacor, Inc.11%
Qfix11%

Company = labeler of record on GUDID. 9 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Multimodality transfer table topAIRPALAIR-MATTAIR_MATTAIR MATTPremierPro Air Transfer MatsPremierPro Air Transfer MatPremierPro Air TrasnsferSingle Patient Use HoverMattHoverMatt SPU Plus HoverCoverTransMattHoverSlingHoverSling Repositiong SlingHoverSling Repositiong Sling-TVASizeWise MattHoverMatt

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, Powered59
FRZDEVICE, PATIENT TRANSFER, POWERED56
FMRDevice, Transfer, Patient, Manual20
INKStretcher, Wheeled, Powered7
IXQTable, Radiographic, Stationary Top1
FSALift, Patient, Non-Ac-Powered1

GMDN & GCC registration

  • GMDN code 37160 · non‑implantable
  • Single‑use 11% · sterile 0% · Rx‑only 6% · OTC 1%
  • 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) · 59Length (Inch) · 13

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

How many patient transfer system, powered products are registered in the US?

111 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Patient transfer system, powered", from 9 companies. The largest labeler is Hovertech International with 53% of records.

Which FDA product codes apply?

FRZ (Device, Patient Transfer, Powered), FRZ (DEVICE, PATIENT TRANSFER, POWERED), FMR (Device, Transfer, Patient, Manual), INK (Stretcher, Wheeled, 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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