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General| Detector Size | 24 cm x 29 cm |
|---|---|
| Pixel Pitch | 70 μm |
| Image Acquisition | Full Field Digital Mammography (FFDM) |
| X-ray Generator | High Frequency Generator |
| Anode Material | Molybdenum or Rhodium |
| mA Range | Up to 100 mA |
| Compression Force | Up to 200 N (45 lbs) |
| Magnification | 1.8x |
| Workstation Compatibility | DICOM 3.0 |
| Detector Technology | Amorphous Selenium (a-Se) Direct Conversion |
Defines system purpose, indications, contraindications, and safety warnings.
Covers cybersecurity statements and quality control requirements.
Defines user roles, qualifications, and training requirements.
Provides a glossary of terms and acronyms used in the manual.
Defines the meaning of warning, caution, and note indicators used in the manual.
Provides crucial safety warnings and precautions for system operation.
Details safety measures and guidelines related to radiation exposure.
Explains the function and use of emergency off switches.
Covers system compliance requirements and manufacturer responsibilities.
Shows diagrams indicating the location of system labels.
Provides an overview of the Selenia system and its main components.
Details the system's power controls and circuit breakers.
Details components, controls, and display of the acquisition workstation.
Explains controls and displays for the tubestand, C-arm, and compression device.
Step-by-step guide for starting up the Selenia system.
Outlines monthly functional tests for system controls.
Provides instructions for restarting the system, including after emergency off.
Provides steps for properly shutting down the Selenia system.
Describes the patient face shield, its installation, and removal.
Details types, installation, removal, and maintenance of compression paddles.
Explains installation and removal of the magnification platform.
Details installation, removal, and alignment of the crosshair device.
Introduces the three main screens of the user interface.
Covers selecting patients, procedures, and acquiring images.
Details the Patient Views screen and image enhancement tools.
Explains how to accept or reject acquired images.
Provides general guidelines and precautions for cleaning the system.
Presents a table of user preventive maintenance tasks and frequencies.
Provides dimensional specifications for system components.
Provides specifications for electrical input to system components.
Details technical specifications for the tubestand, C-arm, and compression.
Lists technical specifications for the image receptor.
Provides general info on Selenia systems in mobile environments.
Lists safety warnings and precautions specific to mobile installations.
Details specifications for mobile Selenia systems, including environment and electrical.
Offers a checklist for testing system integrity after relocation.
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