MEDX

Call us at 800.323.6339
MEDX is here when you need us most

MEDX Mobile InteCam® Gamma Camera System

Contact MEDX Now for:
More Information Service Parts

Documents

 Demonstrations:

For more information on the MEDX InteCam® for GE Mobile gamma camera please call Eric Ellingson at 800.323.6339 or email sales@medx-inc.com

Click here to learn more about MEDX’s responsive nuclear medicine service options.
 

MEDX remanufactures the Starcam 300AM Mobile camera into the MEDX Mobile InteCam® System by integrating a state-of-the-art NuQuest® acquisition and processing workstation. This can be done as an upgrade to a nuclear camera currently in the field or can be purchased as a complete system directly from MEDX.  The remanufacturing process replaces virtually all of the OEM electronics with new electronics, reducing costly service calls. The process also includes a completely new crystal assembly and a new, fast and reliable NuQuest® computer. The exclusive MEDX remanufacturing process results in increased performance, better specifications and reliable diagnostic image quality.

Features

  • Ability to export DICOM 3.0 to any PACS or DICOM compliant system
  • Circular 300mm FOV

Available Options

  • Convenience Devices
  • Extended Warranties
  • Fully Equipped Hot Lab
  • New Cardiac Gate
  • Patient Comfort Devices
  • Printers
  • Professional Accreditation Support Services (PASS)
  • Software Add-Ons
  • Uninterruptible Power Supply

“A remanufacturer as defined in 21 CFR 820.3 (w) is any person who processes, conditions, renovates, repackages, restores, or does any other act to a finished device that changes the finished device's performance or safety specifications or intended use.  Remanufacturers are considered manufacturers. As such, these manufacturers are subject to inspection by FDA and shall meet the applicable requirements of the medical device QS regulation. These manufacturers shall establish and implement quality systems to assure the safety and effectiveness of the devices that are distributed…”
Source: Good Manufacturing Practices (GMP)/Quality System Regulation.  2004 U.S. Food and Drug Administration. 28 Jan 2004.
http://www.fda.gov/CDRH/DEVADVICE/32.html/