Logiq 7 ultrasound manual

Set points at appropriate locations. Pull up video clip of beating heart b. Press M for m-mode c. Press Scan Area to move cursor d. Control Panel Map. Controls are grouped together by function for ease of use. See the callouts for this figure on the following page. Cursor, Clear,. Sep 17, GE Healthcare. Regulatory Requirement. Chapter 4. Regulatory Requirements. Chapter 5. Table of Contents. Chapter 6.

Chapter 1. Chapter 7. Mar 11, Leading provider of outcome-based solutions in healthcare. Primary care. Avg Selling Price. Women's Health. Surgical C-Arms. Image Guided FastWorks principles guide NPI's.

Sep 15, Use and Maintenance of G. Revision History. Version Reason for Revision. Page 7 of In general, there are two types of soft Menu keys: Paddle Switch and adjustable knobs. Aug 14, Direction Rev. Installation Guide. AC Adapter. Select the desired biopsy kit. Page 56 Before scanning, verify the needle can be visualized within the imaging plane.

User appropriate needle length to reach target area. Page 58 Disposable components are packaged sterile and are single-use only. Do not use if integrity of packing is vilated or if expiration date has passed. Page 59 3. Attach the biopsy bracket to the probe by sliding the bracket over the end of the probe until it clicks or locks in place.

Place an adequate amount of coupling gel on the face of the probe. Page 60 Use the rubber bands supplied to hold the sheath in place.

Applying Sanitary Sheath 6. Snap the fixed or adjustable needle clip onto the biopsy guide bracket. Fixed Needle Clip Attachment a. Page 61 This is because the guide allows variable angles. For in-plane needle guides, steps 8 and 9 are not applicable. Page 62 9. Place the needle barrel into the needle clip with the desired gauge facing the needle clip and snap into place.

Page 63 Push the knob down Figure b into the desired slot to secure the angle position of the needle guide attachment. Page 64 Hold the side a and tuck down the needle guide side b until it clicks or locks in place. Page 65 Use the rubber bands supplied to hold the sheath in place. Snap the needle guide onto the biopsy guide bracket.

Page 66 Figure Needle Barrel 9. Page 67 1. Hold the other side and push out the needle clip attachment side. See Figure Remove the biopsy guide Prevent damage to the probe lens with finger nails. Page 68 Push the knob portion of a sleeve in the direction of the arrow. The needle is released from the assembly. Push the probe and the assembly in the direction of the larger arrow to remove the needle.

Page 69 Figure Attachment Filling Removal a. Probe Head b. Attachment c. Filling Removal Tool 3. Clean, then disinfect the probe. NOTE: Ensure that protective gloves are worn.

Page 70 Figure Endocavitary Probe with Sheath a. Probe Handle b. Sanitary Sheath c. Probe Body 5. Rub a finger over the tip of the probe to ensure all air bubbles have been removed.

Page 71 3. Page 72 1. Press the needle guide onto the probe shaft and push it forward until the small swelling of the needle guide cacthes in the notch at the probe tip. Page 74 4.

Place the needle in the guide between the needle barrel and needle clip. Direct it into the area of interest for specimen retrieval. Therefore, both the operator and probe needs to be sterile.

Page 77 5. Depending on the type of procedure, use either sterile water or sterile gel on the sheath cover. Select Register. Select the probe to start scanning or select Exit, Esc, Scan, or Freeze. Perform the exam. Page Patient Screen 1. Image Management 2. Function Selection 3. Dataflow Selection 5. Exit 6. Patient Information 7. Category Selection 8. Exam Information 9. Scan Assistant Program Page 82 Ensure you have selected a dataflow. Exit Used to exit the Patient Menu.

Page 83 All possible information needs to be entered. NOTE: Img. Archived means that the exam was backed up to external media by EZBackup or Export. Make sure the correct patient identification appears on all screens and hard copy prints. Page 86 Read. Press the right Set key to select the patient. Press the left Set key to bring up the print menu. Select Print and press the right Set key to print the patient list. Page Optimizing The Image Velocity Scale live imaging only , baseline shift, dynamic range, and invert if preset.

Upon deactivation, the spectrum is still optimized. Tilt is not available on Linear probes. Page 90 Suppression Suppresses the noise in the image. Speed of Sound Changes the transmitted speed of sound for various tissue types. Frame Average Averages color frames.

Transparency Map Brings out the tissue behind the color map. Page 92 PDI does not map velocity, therefore it is not subject to aliasing. Page Doppler Mode Controls Traces the average mean and peak velocities in realtime or frozen Spectral Trace images. Cycles to Average The average value over a number of cycles from Trace Sensitivity Adjust the trace to follow the waveform for signal strength. Page 95 Activates the menu to select which calculations are automatically calculated.

Auto Calcs Activates the calculation automatically which you select in the Modify Auto Calculation when the system is in a state of freeze or live. Page 3D Mode 6. To complete the 3D scan, press End Trackball key. Page Other Controls To zoom an image, adjust Zoom. A reference image appears in the lower, left-hand section of the display. To exit zoom, adjust Zoom until the reference zoom image is removed or press B-Mode.

Page 98 but not from the worksheet. Press Freeze. Move the Trackball. Page 99 Clear key. Press Set on the keyboard or Scan on the Touch Panel to exit without erasing the body pattern. Page To create a Fast Key, press the F5 key and follow the on-screen prompts. To start a Fast Key, press the F6 key and follow the on-screen prompts.

Page 5. Thumbnail Size 3. Page Measurement And Analysis The user should consider contraindications for the use of a calculation or chart as described in the scientific literature.

The diagnosis, decision for further examination, and medical treatment must be performed by qualified personnel following good clinical practice. Current functionality is displayed on the lower-right corner of the monitor. Pointer Key. Select to display a pointer on the monitor.

Page To rotate through and activate previously fixed calipers, adjust Cursor Select. Page To erase the ellipse and the current data measured, press Clear once. The original caliper is displayed to restart the measurement. To trace the measurement area, move the Trackball around the anatomy. A dotted line shows the traced area. To complete the measurement, press Set. Paper documentation may be ordered by using a form in the Quick Guide.

They do not include sonographic training or detailed clinical procedures. Introduction Principles of Operation Medical ultrasound images are created by computer and digital memory from the transmission and reception of mechanical high-frequency waves applied through a transducer. KG TEL: 33 KG TEL: 49 Chapter 2 Safety Describes the safety and regulatory information pertinent for operating this ultrasound system.

Safety Safety Precautions Precaution Levels Icon description Various levels of safety precautions may be found on the equipment and different levels of concern are identified by one of the following flag words and icons which precede the precautionary statement.

Safety Important Safety Considerations The following topic headings Patient Safety, and Equipment and Personnel Safety are intended to make the equipment user aware of particular hazards associated with the use of this equipment and the extent to which injury can occur if precautions are not observed.

Additional precautions may be provided throughout the manual. The user must be thoroughly familiar with the instructions and potential hazards involving ultrasound examination before attempting to use the device.

Training assistance is available from GE Medical Systems if needed. The equipment user is obligated to be familiar with these concerns and avoid conditions that could result in injury.

Diagnostic Equipment malfunction or incorrect settings can result in information measurement errors or failure to detect details within the image. The equipment user must become thoroughly familiar with the equipment operation in order to optimize its performance and recognize possible malfunctions. Applications training is available through the local GE representative. Added confidence in the equipment operation can be gained by establishing a quality assurance program.

CAUTION Allowing the machine to transmit acoustic output with the probe not in use or in its holder can cause the transducer to build up heat. Preset Auto Freeze to freeze the image when the machine is not in use. Mechanical hazards Electrical Hazard. Take extra care not to drop transducers and avoid contact with sharp or abrasive surfaces.

A damaged housing, lens or cable can result in patient injury or serious impairment or operation. Always minimize exposure time and keep ultrasound levels low when there is no medical benefit. Observe the acoustic output display and be familiar with all controls affecting the output level. Do not use with Defibrillator. This equipment does not have a defibrillator approved applied part. If any defects are observed or malfunctions occur, stop operating the equipment and perform the proper action for the patient.

Inform a qualified service person and contact a Service Representative for information. There are no user serviceable components inside the console.

Refer all servicing to qualified service personnel only. GE is NOT responsible for any lost patient information or for lost images. The HDD is not considered a permanent storage device. Backup data on a regular basis. Develop emergency procedures to prepare for such an occurrence. DANGER The concerns listed below can seriously affect the safety of equipment and personnel during a diagnostic ultrasound examination.

Safety Precautions Related Hazards continued. Risk of explosion if used in the presence of flammable anesthetics. Safety Related Hazards continued Biological For patient and personnel safety, be aware of biological Hazard hazards while performing invasive procedures.

Follow sterile procedures when appropriate. Refer to Chapter 17 Probes and Biopsy for probe use and care instructions. Sensitive users and patients must avoid contact with these items.

Always turn off acoustic output or freeze the image when not in use. The system is equipped with an Auto Freeze feature which disables acoustic output and freezes the image when the machine is not in use. Touching other moving parts other than the Control Panel may cause personal injury. Performing data backup to any device is recommended.

This must be performed by qualified service personnel only. First, perform EZBackup to save the images. Blocking the ventilation slots prevents proper airflow and may result in fire, electric shock, or equipment damage. Small objects or liquid may accidentally fall through the ventilation slots into the cabinet or spill into the cabinet which may result in fire, electric shock, or equipment damage.

Call a Service Representative for information. This includes both objects and people. These pixels may appear as a slightly light or dark area on the screen. This is due to the characteristics of the panel itself, and not the product.

When the screen becomes dark or begins to flicker, contact a qualified Service Representative for information. Safety Device Labels Label Icon Description The following table describes the purpose and location of safety labels and other important information provided on the equipment.

Can be used in operating room environment. Connection of additional protective earth conductors or potential equalization conductors is not necessary in most cases and is only recommended for situations involving multiple equipment in a high-risk patient environment to provide assurance that all equipment is at the same potential and operates within acceptable leakage current limits.

An example of a high-risk patient would be a special procedure where the patient has an accessible conductive path to the heart such as exposed cardiac pacing leads. Circuit breaker label of console and front panel if applicable. Please contact an authorized representative of the manufacturer for information concerning the decommissioning of your equipment. No hazardous substance, above the maximum concentration value, is present.

Indicates the presence of hazardous Probe substance s above the maximum concentration value. Do not use the following devices near Rear Panel this equipment: cellular phone, radio receiver, mobile radio transmitter, radio controlled toy, broadband power lines, etc. Use of these devices near this equipment could cause this equipment to perform outside the published specifications. Keep power to these devices turned off when near this equipment. Pay attention to the monitor arm Monitor arm.

This product consists of devices that Rear of console may contain mercury, which must be recycled or disposed of in accordance with local, state, or country laws. Within this system, the backlight lamps in the monitor display, contain mercury. This additional safety precaution prevents exposed metal parts from becoming LIVE in the event of an insulation failure.

The equipment may cause radio frequency interference to other medical and non-medical devices and radio communications. To provide reasonable protection against such interference, this product complies with emissions limits for a Group 1, Class A Medical Devices Directive as stated in EN However, there is no guarantee that interference will not occur in a particular installation. NOTE: The manufacturer is not responsible for any interference caused by using other than recommended interconnect cables or by unauthorized changes or modifications to this equipment.

Use of cables not properly shielded and grounded may result in the equipment causing radio frequency interference in violation of the FCC regulations. You can only view or download manuals with.