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Device Explorer · FDA GUDID · GMDN 17230

Tourniquet cuff, reusable

A band-like device that is applied around an extremity (arm or leg) and connected to a tourniquet unit to apply a controlled pressure to restrict blood circulation and prevent normal blood flow to or from the distal area during a surgical intervention or serio

US‑registered devices220in commercial distribution
Companies14labelers on GUDID
Single‑use1%of device records
Sterile1%labelled sterile
Prescription65%Rx‑only share
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Share of device records

Delfi Medical Innovations Inc5726%
Vbm Medizintechnik Gmbh4018%
Orantech Inc.3516%
Zhejiang Longyou Lande Medical Technology Co., Ltd.3315%
Stryker Corporation2210%
Zimmer Orthopaedic Surgical Products, Inc.2110%
Asp Global, Llc42%
Accurate Surgical & Scientific Instruments Corporation21%

Top labelers

CompanyDevicesShare
Delfi Medical Innovations Inc5726%
Vbm Medizintechnik Gmbh4018%
Orantech Inc.3516%
Zhejiang Longyou Lande Medical Technology Co., Ltd.3315%
Stryker Corporation2210%
Zimmer Orthopaedic Surgical Products, Inc.2110%
Asp Global, Llc42%
Accurate Surgical & Scientific Instruments Corporation21%
Secondperspective Ltd.10%
Bv Medical10%
Magnum Medical, Inc.10%
Ace Surgical Supply Co., Inc.10%

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

Brand names on the register (sample)

Color CuffReusable Conical CuffReusable Tourniquet CuffOrantechSuji BFRn.a.Silicone Double Cuff for legN/ABV MedicalASSIASP MEDICALMagnum MedicalACEPetite-Fit (Small Adult), ReusablePedi-Fit ReusableEasi-Fit Reusable

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

FDA product codes

CodeNameDevices
KCYTourniquet, Pneumatic221
KCYTOURNIQUET, PNEUMATIC31
GAXTourniquet, Nonpneumatic5
QGXGeneral Use Pneumatic Tourniquet1
GAXTOURNIQUET, NONPNEUMATIC1
DWSINSTRUMENTS, SURGICAL, CARDIOVASCULAR1

GMDN & GCC registration

  • GMDN code 17230 · non‑implantable
  • Single‑use 1% · sterile 1% · Rx‑only 65% · OTC 15%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Inch) · 107Length (Centimeter) · 60Width (Inch) · 31

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

How many tourniquet cuff, reusable products are registered in the US?

220 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Tourniquet cuff, reusable", from 14 companies. The largest labeler is Delfi Medical Innovations Inc with 26% of records.

Which FDA product codes apply?

KCY (Tourniquet, Pneumatic), KCY (TOURNIQUET, PNEUMATIC), GAX (Tourniquet, Nonpneumatic), 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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