Consulting Wallah › Device Explorer › Other devices › Arterial tourniquet, pneumatic
Device Explorer · FDA GUDID · GMDN 65141

Arterial tourniquet, pneumatic

An inflatable cuff with fastening mechanism intended to be placed around a patient's limb (arm or leg) and pneumatically inflated from an integrated small gas cartridge to reduce and/or occlude arterial blood circulation to the distal portion of the limb durin

US‑registered devices303in commercial distribution
Companies3labelers on GUDID
Single‑use100%of device records
Sterile99%labelled sterile
Prescription99%Rx‑only share
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Share of device records

Provision28995%
Group Supply Organization Medical Technology(Shanghai) Ltd124%
First Care Products Ltd21%

Top labelers

CompanyDevicesShare
Provision28995%
Group Supply Organization Medical Technology(Shanghai) Ltd124%
First Care Products Ltd21%

Company = labeler of record on GUDID. 3 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

The Quick-T tourniquetQuick-TGSOResilientmacSourceMark MedicalGSO MedicalAA MedicalASP MedicalDelfi MedicalExpressAireHammarplast MedicalZimmerStrykerBackorder SolutionsMedProtect

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

FDA product codes

CodeNameDevices
KCYTourniquet, Pneumatic301
QGXGeneral Use Pneumatic Tourniquet2

GMDN & GCC registration

  • GMDN code 65141 · non‑implantable
  • Single‑use 100% · sterile 99% · Rx‑only 99% · OTC 0%
  • 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 arterial tourniquet, pneumatic products are registered in the US?

303 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Arterial tourniquet, pneumatic", from 3 companies. The largest labeler is Provision with 95% of records.

Which FDA product codes apply?

KCY (Tourniquet, Pneumatic), QGX (General Use Pneumatic Tourniquet)

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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