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MEDX InteCam® for Siemens Orbiter Gamma Camera


MEDX Intecam™ for Siemens OrbiterOverview

MEDX remanufactures the Siemens Orbiter into the MEDX InteCam® for Siemens Orbiter gamma camera by integrating a state-of-the-art NuQuest® acquisition and processing system. 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 eliminates many of the original manufacturer’s electronics, reducing potential service calls, and includes a completely new crystal assembly, a rebuilt detector and a new fast, reliable PC. The exclusive MEDX remanufacturing process results in increased performance, better diagnostics and faster imaging and data processing for all of your nuclear cardiology and general nuclear medicine procedures.

Features
  • Improved energy, linearity and uniformity corrections
  • Real-time isotope display during all acquisitions
  • Intrinsic and extrinsic uniformity correction tables for any isotope-collimator pair
  • Latest generation USB V2 Acquisition Interface
  • Circular 387mm 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

For more information on the MEDX InteCam® for Siemens Orbiter gamma camera please call Jessica Romig at 800.323.6339 or email sales@medx-inc.com

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


“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/