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1. INTRODUCTION
The information in this section is PPM System check. It should ensure that the clinical user can using
the system without errors.
2. VERIFICATION ITEMS
2.1. POWER-ON/OFF
Switch off entire system.
Check that the NT shut-down dialogs come up on the data monitor.
Switch on system.
Verify normal power on.
Check that an 'Emergency Patient' comes up on the Patient Data Monitor after start-up.
2.4. CUSTOMIZATION
Select each application procedure on the Patient Data Monitor and check that these are valid.
Look at symbol in the lower-left corner of the monitor: green open circle = valid, red cross = invalid.
If many physicians have been customized: check a number of representing procedures.
2.6. FLUOROSCOPY
Check if the available fluoroscopy flavors operate correctly.
Pay attention to:
X-ray on indicator.
Control loop (minimum / maximum kV/mA values) during Normal and High level fluo.
Patient Entrance Exposure rate (PEE) and SID correction (if applicable).
High level fluo buzzer / high level fluo control / fluo buzzer (if applicable).
Collimator shutters / wedge filter (shutters and wedges on last image hold).
Patient orientation.
FD field size.
LIH (if programmed).
2.7. EXPOSURE
Check if exposure operates correctly.
Try different procedures, with short and long runs.
Try a subtraction run.
Pay attention to:
X-ray on indicator.
Collimator shutters / wedge filter (during long run).
Control loop (minimum / maximum kV/mA values) during exposure.
2.8. MOVEMENT
Check stand and patient support movement.
Pay attention to:
Patient safety (bodyguard sensor, current limitation).
Emergency stop button (see 2.1, Power-on/off).
Range.
Smooth movement.
Tip: The Field Service Framework has procedures to program and run (complex) stand movements.
These procedures can be found in: Diagnostics > Geometry > Functional Test > Integrated
Subsystem Test.
2.10. ARCHIVING
Check if patient data can be archived.
(Don't forget to remove this patient when you have finished the verification!)
2.12. OPTIONS
Check if the requested options are present and working, such as:
Multivision
Physio display
3D-RA
Injector
Ultrasound
Paper printer
Film printer
Intercom
Video recorder
FD 10 PPM METHOD STATEMENT Part 2
1. INTRODUCTION
This document gives the set of tests, checks and measurements on system level that are relevant for
system acceptance.
Acceptance tests are done after System Verification. The difference is:
System Verification:
Check that the system work without errors, so that the clinical user can start without problems. Only
functional checks, no measurements.
System Acceptance:
Check that the system’s performance is in accordance to regulations, standards and specifications.
The performance is measured and the measured values must be within defined limits.
Some tests are mandatory (e.g. for DHHS regulations).
For test procedures and limits, references are given to either on-line service procedures or service
documents.
2. ACCEPTANCE ITEMS