Consulting Wallah › Device Explorer › Other devices › Radial artery compression device
Device Explorer · FDA GUDID · GMDN 58704

Radial artery compression device

A device intended to provide compression for haemostasis to the puncture site on a patient having undergone radial artery catheterization, and can be used as an alternative to direct hand pressure. It typically consists of one or more pad/strap(s), which may a

US‑registered devices74in commercial distribution
Companies15labelers on GUDID
Single‑use100%of device records
Sterile99%labelled sterile
Prescription62%Rx‑only share
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Share of device records

Merit Medical Systems, Inc.3041%
Teleflex Incorporated79%
Vasoinnovations Inc.68%
Semler Technologies, Inc.68%
Tianck Medical Co., Ltd.57%
Medas Inc45%
Tricol Biomedical, Inc.34%
Tz Medical, Inc.34%

Top labelers

CompanyDevicesShare
Merit Medical Systems, Inc.3041%
Teleflex Incorporated79%
Vasoinnovations Inc.68%
Semler Technologies, Inc.68%
Tianck Medical Co., Ltd.57%
Medas Inc45%
Tricol Biomedical, Inc.34%
Tz Medical, Inc.34%
Medline Industries, Inc.34%
Medtronic, Inc.23%
Enodar Medical (Shanghai) Co.,Ltd.11%
St. Jude Medical, Inc.11%

Company = labeler of record on GUDID. 15 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Radial artery closure bandSEQSEALRadiStop™Finale®HemCon® ChitoPulse™, 15 inchHemCon® ChitoPulse™, 12 inchHemCon® ChitoPulse™, 9 inchVASOBandVasoStat Hemostasis DevicePH BandMEDADVARC Adjustable Radial CuffTRAcelet™Syvek Radial BandMEDLINEPreludeSYNC™

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

FDA product codes

CodeNameDevices
DXCClamp, Vascular44
DXCCLAMP, VASCULAR39
KCYTourniquet, Pneumatic5
FRODressing, Wound, Drug3
GAXTOURNIQUET, NONPNEUMATIC2
GAXTourniquet, Nonpneumatic1

GMDN & GCC registration

  • GMDN code 58704 · non‑implantable
  • Single‑use 100% · sterile 99% · Rx‑only 62% · 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

Length (Centimeter) · 12Circumference (Centimeter) · 6

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

How many radial artery compression device products are registered in the US?

74 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Radial artery compression device", from 15 companies. The largest labeler is Merit Medical Systems, Inc. with 41% of records.

Which FDA product codes apply?

DXC (Clamp, Vascular), DXC (CLAMP, VASCULAR), KCY (Tourniquet, Pneumatic), FRO (Dressing, Wound, Drug)

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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