Consulting Wallah › Device Explorer › Equipment & monitoring › Stationary angiographic x-ray system, digital
Device Explorer · FDA GUDID · GMDN 37623

Stationary angiographic x-ray system, digital

A stationary diagnostic fluoroscopic x-ray system specifically designed to optimize the capability of users to visually and quantitatively evaluate the anatomy and function of blood vessels of the heart, brain and other organs, as well as the lymphatic system.

US‑registered devices178in commercial distribution
Companies11labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription46%Rx‑only share
ShareLinkedIn

Share of device records

Shimadzu Corporation8849%
Philips Medical Systems Nederland B.V.4224%
Siemens Healthcare Gmbh2011%
Ge Medical Systems106%
Canon Inc.42%
Omega Medical Imaging, Llc42%
Ge Hualun Medical Systems Co., Ltd42%
Nrt - Nordisk Røntgen Teknik A/S21%

Top labelers

CompanyDevicesShare
Shimadzu Corporation8849%
Philips Medical Systems Nederland B.V.4224%
Siemens Healthcare Gmbh2011%
Ge Medical Systems106%
Canon Inc.42%
Omega Medical Imaging, Llc42%
Ge Hualun Medical Systems Co., Ltd42%
Nrt - Nordisk Røntgen Teknik A/S21%
Imris Imaging, Inc.21%
Shanghai United Imaging Healthcare Co., Ltd.11%
Siemens Shenzhen Magnetic Resonance Ltd.11%

Company = labeler of record on GUDID. 11 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

uAngioIntelli-C Right Side Suspended TableIntelli-C Left Side Suspended TableINTERVENTIONAL ANGIOGRAPHY SYSTEMTriniasTRINIASDAR-8000iBRANSIST safireARTIS genio floorARTIS icono.explore floorARTIS icono ceilingARTIS icono floorARTIS icono biplaneARTIS phenoArtis zee biplane MNArtis zee floor MN

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

FDA product codes

CodeNameDevices
OWBInterventional Fluoroscopic X-Ray System128
JAASystem, X-Ray, Fluoroscopic, Image-Intensified70
JAASystem, x-ray, fluoroscopic, image-intensified55
OWBInterventional fluoroscopic x-ray system54
IZISystem, x-ray, angiographic43
JAKSystem, x-ray, tomography, computed22

GMDN & GCC registration

  • GMDN code 37623 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 46% · 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 stationary angiographic x-ray system, digital products are registered in the US?

178 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Stationary angiographic x-ray system, digital", from 11 companies. The largest labeler is Shimadzu Corporation with 49% of records.

Which FDA product codes apply?

OWB (Interventional Fluoroscopic X-Ray System), JAA (System, X-Ray, Fluoroscopic, Image-Intensified), JAA (System, x-ray, fluoroscopic, image-intensified), OWB (Interventional fluoroscopic x-ray system)

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?

Add stationary angiographic x-ray system, digital to the RFQ basket or use the form below with quantity, specification and delivery location; the Network returns comparable quotes from verified suppliers in 2–5 working days.

Request quotes for Stationary angiographic x-ray system, digital

Hospitals, pharmacies and distributors anywhere: tell us what you need and the Consulting Wallah Network returns comparable quotes from verified suppliers. No fee for buyers.

Buying stationary angiographic x-ray system, digital for a hospital group?Free executive assessment: we benchmark your prices and tender structure against the Network.
Book the free assessment

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.

Get quotes →