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IQ Portable X-Ray System

Overview


Medical Equipment & Lab Supplies
Pennsylvania, United StatesPosted: August 21, 2026Deadline: August 31, 2026

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SUMMARY


A Pennsylvania government authority is seeking a portable digital X-ray system or approved equivalent, including installation, training, warranty, maintenance, and imaging software. Questions are due August 27, 2026, with proposals due August 31, 2026.

DESCRIPTION


A government authority in Pennsylvania seeks one new FDR GO iQ Portable X-Ray System with an FDR D-EVO III C35 14 x 17-inch CSI wireless detector, or an approved equivalent. The procurement includes installation, training, warranty coverage, annual preventative maintenance, and all components required for instructional and clinical radiographic imaging applications.

The system is expected to include programmable passcode and keyless activation, centering lights, an integrated wireless detector, Speed Link X-ray Control Software, Dynamic Visualization II image processing technology, a caesium iodide scintillator with an amorphous silicon readout layer, antibacterial HYDRO AG coating, a 684-pound distributed detector load capacity, three detector batteries, and a two-slot charger.

Required software and imaging features include virtual grid software, patient registration and exam management, image magnification, zoom, edge enhancement, annotation tools, and automatic trimming and shuttering functions. Vendor questions must be submitted by August 27, 2026, and proposals are due by August 31, 2026.

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Frequently asked questions


When is the submission deadline?
Submissions are due August 31, 2026.
Who is a good fit for this opportunity?
  • Medical imaging equipment manufacturers or authorized distributors
  • Experience supplying portable digital radiography systems to government or healthcare institutions
  • Qualified technicians capable of installation, training, preventative maintenance, and warranty support
  • Capability to provide wireless detectors, compatible software, batteries, chargers, and related components
  • Demonstrated compliance with applicable medical device procurement and safety requirements

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