Planned Maintenance
- Planned Maintenance (PM) schedule overview
  Planned Maintenance (PM) tasks are developed from design requirement and operations/use assumptions to provide for the minimum required maintenance that maintains specified equipment design performance, high image quality, and safety. GE Healthcare (GEHC) advanced service methods are developed to maximize efficiency and use system access time as productively as possible, as described in the lifecycle maintenance statement.
- PM Procedures
  - Deionization procedure
  - Emergency Stop (E-Stop) planned maintenance
  - Checking InSite connectivity and ProDiags
  - Inspecting the cryogen vent
    Inspect the cryogen vent glass connection and clamp for damage, and weep hole for debris.
  - Checking InSite Remote Service Platform (RSvP) connectivity and ProDiags functionality
    Make sure the Remote Service Platform (RSvP) has connectivity and ProDiags is functioning properly.
  - Checking the oxygen monitor
    References to various Oxygen Monitor Subsystem Manuals.
  - Doing an MRU yearly service check (MRU, ERU, or EDU PM testing matrix)
    The model number is listed on the side of the MRU, ERU, or EDU. Refer to the appropriate vendor manual available from the online documentation library for applicable testing procedures.
  - Checking the pneumatic patient alert system
    Makes sure the stand-alone pneumatic patient alerts system is operating properly.
  - Checking and filling hydraulic fluid
    Checks and adjusts the hydraulic fluid level for the dockable patient table.
  - Body coil air flow functional check
  - Cleaning or replacing the body coil blower air flow filter
    Clean and/or replace the body coil blower air flow filter.
  - Checking the patient handling system with the laser leveling tool
    The proper alignment of the entire patient handling system is important for good image quality output from the GE MR scanners.
  - MDP power and ground and battery replacement label check
    MDP power and ground connections must be tight in order to avoid system failures.
  - Checking and adjusting the patient intercom functionality
    GOC Audio Assembly (GOCAA) controls are adjusted at factory for best sound quality. This document describes how to check and confirm volume and quality of sound heard from speaker in the magnet bore and from speaker at the Scan Control and Intercom Module (SCIM). Directions for sound adjustments are also provided if needed.
  - Patient table movement verification
    Makes sure the patient table controls operate correctly.
  - Cradle/table release block adjustment/cradle egress functionality
    Adjust the cradle release block position and the cradle release block retraction.
  - Doing the Leak Sensor functional check
    Test the functionality of the leak sensors.
  - Doing the UPM functional check (head and body)
    Do the UPM head and body functional check to make sure the measured RF power is within the expected range.
  - Dual drive quadrature tool
  - Doing DQA calibration
    The DQA tool determines proper gradient polarity and proper gradient wiring by scanning a series of axial and coronal images of the DQA III phantom.
  - Testing PAC leakage current
    Measure and record the PAC leakage current data.
  - Checking the gradient and system PDU power and ground connection
    PDU power and ground connections need to be tight in order to avoid system failures.
  - Setting the time, time zone, and date
    Set the time, time zone, and date in Guided Install.
  - Replacing and cleaning the blower box filter
    Clean and replace the blower box filter.
  - Heat exchanger cabinet installation and FRU replacements
  - Installing and checking ECG leads
    Checking ECG leads.
  - Checking the GOC battery replacement
    Check the battery replacement sticker on the GOC.
  - T-file cleanup
  - Inspecting the cryocooler adsorber
  - Checking the RF screen room door
    Make sure the RF screen room door is functioning correctly.
  - Cleaning and replacing P-port receptacles (ODU connectors)
    The P-Port receptacle must be cleaned and lubricated on each of the system P-ports.
  - Doing a compressor pressure check
    Do a check of the cryocooler compressor supply pressure.
  - GE OR-compatible MR table option
- E-Reporting tool

Discovery MR750 3.0T System Service Methods
5690009-2EN Revision 4
Object ID: 00000018WIA305FC410GYZ
Topic ID: id_2004455 Version: 6.1
Date: Jul 13, 2021 4:10:15 PM

ODU connector cleaning

About this task

The P-Port receptacle must be cleaned and lubricated on each of the system P-ports (P1 and P2 on the LPCA and P3 and P4 on the 32-channel table). Also, the coil connector must be cleaned and tested for proper fit to each P-port receptacle.

Procedure

Important: Use only the cotton swabs provided with the P-Port Spindle Lubrication Kit to clean the spindle tip. Clean with a dry swab. Do not use alcohol or cleaning products when cleaning the spindle tip. Do not apply any lubricant to the spindle tip. Avoid bending any pin contact.
Use the cotton swabs included in the P-Port Spindle Lubrication Kit to clean the spindle tip on the coil connector of each coil on site, removing all dirty lubricant and dust particles from the spindle tip, especially from the groove. (See the illustrations below.)

Figure 1. Cleaning spindle tip

Figure 2. Cleaning spindle tip groove
Important: Make sure to inspect the lubricant expiration date prior to use. Do not use out of date material.
Clean and lubricate all the system P-port connectors as shown below.

Note: Special lubricant (included in the P-Port Spindle Lubrication Kit) and cotton swabs are required for cleaning and lubricating the P-port receptacle on the scanner.

Figure 3. Cleaning P-Port receptacle with cotton swab

Figure 4. Lubricating with special syringe

Figure 5. Location of pins in P-Port receptacle
During the cleaning process, inspect the receptacle contact surface and remove any debris.
After all the P-Port connectors are cleaned and lubricated, cap and store the syringe with any unused portion in the original labeled packaging for future use. Assure the outer packaging is clean of lubricant, remove the protective gloves, and wash your hands to remove any lubricant residue.
Cap and store the syringe with any unused portion in the original labeled packaging for future use.
After the syringe is empty or has an expired date code, dispose of the syringe according to the SDS provided with the kit.