Spectris Solaris Calibration Verification
Ensure Injection Accuracy and MRI Safety with Annual Calibration Checks
Precise volume and pressure delivery is critical in MRI contrast injections. FDM Enterprises provides professional calibration verification for your Medrad Spectris Solaris system, ensuring peak performance and patient safety.
What We Verify
Plunger position accuracy (A and B sides)
Volume delivery at multiple syringe sizes
Pressure limit functionality
KVO timing and volume
Post-calibration QA scan and report
When to Check
Annually during preventive maintenance
After potentiometer or motor replacement
Following battery or fiber optic repairs
After any major system service event
When injection volumes seem inconsistent
Why Calibration Checks Matter
Accurate contrast delivery for patient safety
Consistent injection volumes across procedures
Compliance with manufacturer specifications
Documented QA reports for regulatory audits
Extended equipment life through proper tuning
FDM Calibration Expertise
25+ years of Service experience
Trained on Medrad Spectris Solaris systems
Comprehensive post-checks QA reports
Fast on-site service across the Southeast US
Frequently Asked Questions
Calibration verification confirms that your Medrad Spectris Solaris injector is delivering accurate contrast volumes and pressures. FDM Enterprises tests plunger position accuracy, volume delivery at multiple syringe sizes, pressure limits, and KVO timing to ensure your system meets manufacturer specifications.
Accurate calibration ensures that patients receive the correct amount of contrast agent during MRI procedures. Improperly calibrated injectors can deliver too much or too little contrast, which can affect image quality and patient safety.
The Spectris Solaris should be checked at least annually during preventive maintenance. Additional checks are recommended after potentiometer or motor replacement, battery or fiber optic repairs, or any major system service event.
We verify plunger position accuracy on both A and B sides, test volume delivery across multiple syringe sizes, confirm pressure limit functionality, check KVO timing and volume, and provide a comprehensive post-calibration QA scan and report.
Yes, FDM Enterprises provides detailed post-checks QA reports documenting all measurements and results. These reports support your facility's regulatory compliance and equipment maintenance records.