MyLabOmega For US Customers: US Federal Law restricts this device to sale, distribution and use by or on the order of a physician. All information included in this manual is relative to the following Esaote ultrasound equipments: MyLabOmega In this manual, all the above mentioned systems are referred to as MyLab Unless specifically noted, sections of this manual pertain to all the systems.
Guarantee The information in this document is the exclusive property of Esaote S.p.A. and is reserved. Reproduction or distribution in any form is strictly prohibited. All rights reserved. All screenshots, pictures and graphics in this manual are used for descriptive purposes only and may be different from what you see on the screen or device.
I N D E X Table of Contents Manufacturer’s Address ................i-iii Important Information ................i-iii Guarantee..................... i-iv Trade Marks....................i-iv EC Declaration of Conformity..............i-v RED Declaration of Conformity ............. i-vi 1 Introduction.................. 1-1 Safety and Standards................1-1 Getting Started ................... 1-1 Probes and Consumables..............
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I N D E X Communication Systems and MyLab..........2-6 Wireless Requirements ................2-7 3 System Overview ................3-1 About the system..................3-1 Intended Use.....................3-1 Clinical Applications and Supporting Probes ........3-1 Patient population..................3-4 Operator profile ..................3-4 Contraindications ..................3-4 System Overview..................3-5 Portable Configuration................3-5 Identifying the Connectors ...............3-6 Installing the Portable Configuration ..........3-8 Accessories for Outdoor Transport..........3-8 Mobile Configuration ................3-9...
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I N D E X System Controls ..................5-2 Control Panel Section ................5-2 EKnob ....................5-4 Trackball ....................5-4 Touchscreen Section................5-5 On/Off Button .................. 5-5 Menu Button..................5-6 Touchscreen..................5-6 TGC Sliding ..................5-9 Information about the Screen Layout ............. 5-9 Heading Area..................
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I N D E X Field AVAILABLE QWERTIES ..........6-13 CINE MODE Folder ..............6-14 APPLICATION PRESET Folder..........6-14 FOOTSWITCH Folder..............6-15 PROBE BUTTONS Folder ............6-15 RAW DATA Folder.................6-15 KEYBOARD BUTTONS Folder ..........6-15 Security.....................6-16 Licenses Manager ...................6-16 License Activation ................6-16 Import/Export Menu................6-18 EXPORT Folder ................6-18 IMPORT Folder ................6-19 System Info .....................6-20 7 Performing an Exam..............7-1...
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I N D E X Connectivity ..................... 9-4 Image Files....................9-5 Software ....................9-5 Biometry....................9-5 Keyboard ....................9-5 Dimensions....................9-5 Weight ....................... 9-5 IP Grade....................9-5 Power supply.................... 9-5 Operating Requirements ................ 9-6 Storage requirements................9-6 Probe Storage Requirements ..............9-6 Standards......................
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I N D E X MyLab - G E T T I N G S T A R T E D...
MyLabOmega family, or when the contents are common to the other MyLab ultrasound systems belonging to the Esaote platform. MyLab Safety and Standards The Safety and Standard manual contains information about the patient's and operator's safety.
NOTE Specifications subject to change without notice. Information might refer to products or modalities not yet approved in all countries. Product images are for illustrative purposes only. For further details, please contact your Esaote sales representative. This manual refers to...
In case of system failure to operate correctly, the operator should contact the nearest Esaote Service Office. Special attention should be dedicated to intra-cavitary probes (e.g. vaginal, rectal or oesophageal probes). They should be cleaned according to established protocols (AIUM guidelines for cleaning probes) and should not be used if there is noticeable self-heating of the probe when operating in air.
I N T R O D U C T I O N a part of a more complex diagnostic process that includes medical history, symptoms and other instrumental examinations. A proper patient ID and exact examination date and time must be always included and must appear on all recorded data and prints.
Use of the product for the purposes other than those intended and expressly stated by Esaote, as well as incorrect use or operation, may relieve Esaote or its agents from all or some responsibility for resultant noncompliance, damage, or injury.
In this manual NOTE points out information of special interest but not NOTE related to risks for patient, operator or device. Manufacturer’s Responsibility Esaote is responsible for the safety, reliability and functioning of this product only if: the user follows all the instructions contained in the system manuals for the use and the maintenance of this system;...
You have acquired a device (“ ”) which includes Esaote S.p.A. DEVICE proprietary software and/or software licensed by Esaote S.p.A. from one or more software licensors (“Software Suppliers”). Such software products (“ ”), as well as associated media, printed materials, and “online”...
For any software updates and/or upgrades installed on the Equipment after installation, the terms herein shall apply in full. License Rights and Limitations With this license, Esaote S.p.A. grants the end user the right to use the on the supplied SOFTWARE...
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I N T R O D U C T I O N the event of equipment transfer to third parties, are requested to notify ESAOTE S.p.A., associate company or authorized distributor of the said transfer by means of the following form, duly compiled, or written notification with the same data as specified in the form.
Esaote central plants, or one of our subsidiaries, or one of our official distributors immediately through the following form, or through a communication reporting the same data contained in this form.
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I N T R O D U C T I O N POST-MARKET SURVEILLANCE FORM ACCIDENT REPORT FORM To: ESAOTE S.p.A. Quality Assurance Department Via Enrico Melen, 77 16152, Genova, Italy [or associate company] [or authorized distributor] ESAOTE system/device name:................
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I N T R O D U C T I O N MyLab - G E T T I N G S T A R T E D 1 - 12...
Chapter 2. Additional Information on Safety This chapter provides additional information on safety specifically for MyLab products. Please read the “Safety and Standards” manual carefully for a complete overview of all safety aspects of products. MyLab Environmental Safety Special waste The system contains lithium-ion batteries.
A D D I T I O N A L I N F O R M A T I O N O N S A F E T Y Electromagnetic Compatibility This system was designed for use in the electromagnetic environments declared in the tables below, in compliance with standard IEC 60601-1- 2:2014 (4 edition).
A D D I T I O N A L I N F O R M A T I O N O N S A F E T Y Use of accessories, transducers and cables other than those specified or WARNING provided by the manufacturer of this equipment could result in increased electromagnetic emissions or decreased electromagnetic immunity of this...
A D D I T I O N A L I N F O R M A T I O N O N S A F E T Y Electromagnetic Immunity for All Medical Equipment MyLab system is intended for use in the electromagnetic environment specified below. The MyLab customer or the user of the system should assure that it is used in such an environment.
A D D I T I O N A L I N F O R M A T I O N O N S A F E T Y MyLab system is intended for use in the electromagnetic environment specified below. The MyLab customer or the user of the system should assure that it is used in such an environment.
A D D I T I O N A L I N F O R M A T I O N O N S A F E T Y Recommended Distances between Radiofrequency (RF) Communication Systems and MyLab As stated in the “Safety and Standards” manual, it is recommended not to use radiofrequency (RF) transmission systems near the ultrasound system.
A D D I T I O N A L I N F O R M A T I O N O N S A F E T Y Wireless Requirements is equipped with built-in wireless capability. MyLab When wireless is active, the operator should make sure to stay at a minimum distance of 20 cm from the rear of the equipment.
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A D D I T I O N A L I N F O R M A T I O N O N S A F E T Y MyLab - G E T T I N G S T A R T E D 2 - 8...
Chapter 3. System Overview is a professional, innovative and versatile real-time high- MyLabOmega resolution ultrasound system. The wide range of probes makes it suitable for many clinical applications. About the system Intended Use is a compact portable system intended to perform diagnostic...
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S Y S T E M O V E R V I E W mC 3-11 including biopsy capabilities P 1-5 P 2-9 P2 5-13 S2MCW S2MPW S5MCW SB2C41 SB3123 SC3123 including biopsy capabilities ...
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System applications are dependent on your system configuration, NOTE transducer and exam type. Not all applications are approved in all Countries. Please refer to your Esaote local representative for further information. MyLab - G E T T I N G S T A R T E D...
Sex: male and female Weight: all weight categories (in terms of Body Mass Index) Height: no limitations Operator profile is designed for operators who are qualified and trained in using MyLabOmega ultrasound systems: Sonographers Cardiologist ...
S Y S T E M O V E R V I E W System Overview has a built-in LCD screen: in this way, the system can be used as MyLab portable configuration. can be supplied with a trolley in its mobile MyLab configuration.
S Y S T E M O V E R V I E W The system is equipped with an external AC/DC adapter and, as an option, with internal batteries. Identifying the Connectors Table 3-2: Connectors on right side Connector Symbol Description EA1÷EA2 Two probe connectors...
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The mains socket is located on the rear side of the system. Connect the AC/ DC adapter to the mains socket. If the system is equipped with the AC/DC adapter, Esaote P/N 151004300 (see label on the AC/DC adapter): Use only the AC/DC adapter provided by Esaote with the...
S Y S T E M O V E R V I E W Installing the Portable Configuration Refer further in this chapter Place the on the work surface using the handle as sloping support. MyLab for information on probe Position the equipment so that the power outlet is easily accessible.
S Y S T E M O V E R V I E W Fig. 3-2: MyLab Fold-away Trolley Before using the system carefully clean it and the fold-away trolley after they CAUTION have been transported outdoor. Mobile Configuration A height-adjustable trolley is available to set in a mobile configuration.
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S Y S T E M O V E R V I E W Fig. 3-3: MyLab Trolley The trolley is not equipped with insulation transformer. NOTE The trolley provides a handle and independent brakes on four wheels to be easily moved.
S Y S T E M O V E R V I E W The peripheral weight may not exceed 3 kg. The shelf could be damaged if CAUTION the peripheral weight exceeds this limit. The weight in the compartment for additional accessories may not exceed CAUTION 3 kg.
S Y S T E M O V E R V I E W Adjust the system into its final position and then lock them to fix the position. This assembly can be pushed up/down to maximize operator comfort. A lever lock is placed on the back of the trolley near the handle. Push the lever and act on the handle to adjust the height of the control panel.
MyLab batteries. A fully charged battery ensures more than one hour of scanning. The battery pack is installed by Esaote personnel. This person will be NOTE responsible for its installation and for ensuring that the system is working properly.
S Y S T E M O V E R V I E W A system which has not been used for a month needs to be charged before using it with the battery. Charge and discharge the battery only when the environment temperature CAUTION is between 15°C and 30°C.
Esaote recommends to replace the battery pack every three years. The battery pack has to be replaced by Esaote personnel. This person will NOTE be responsible for ensuring that the system is working properly.
Switch on again and check whether the MyLab message is still present. If the problem persists, contact Esaote personnel. Error #4 This error indicates that at least one of the batteries has reached the maximum temperature allowed for its working conditions.
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Verify that nothing is blocking the fan functioning, especially on the rear panel. Should the problem persist, contact the Esaote Service department. Error #7 This error indicates that a fault of the internal voltages occurs. The system displays the following message: Error #7: problem with internal voltage.
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S Y S T E M O V E R V I E W MyLab - G E T T I N G S T A R T E D 3 - 18...
Chapter 4. Preparing the System The system will be installed by Esaote personnel. Esaote personnel will be responsible for opening the packaging and ensuring that the system is correctly programmed and operational. The information and procedure provided in this chapter will guide to prepare the system for use.
MyLab usually already mounted and connected. The first mounting and connecting will usually be performed by an Esaote technician. Esaote suggests to contact its Service representative to install any auxiliary NOTE device. Before installing the peripheral devices, make sure that the system is switched off and unplug the power cable from the mains outlet.
P R E P A R I N G T H E S Y S T E M Furthermore, all configurations shall comply with the requirements for medical electrical systems (see IEC 60601-1-1 or clause 16 of the 3rd Edition of IEC 60601-1, respectively).
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B or area C connected by cable (USB, HDMI,...) - Auxiliary device must be powered through a safety insulation transformer complying to IEC 60601. Auxiliary Devices must be approved by Esaote. Auxiliary Devices must also NOTE comply with EN 60601-1-2 safety standard and subsequent amendments or the electromagnetic compatibility.
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The system must be powered so to satisfy the electrical safety requirements, WARNING as specified in the “Safety and Standards” manual. Esaote recommends running a current leakage (patient and environment) test when installing in order to check whether the applicable limits of standard EN60601-1 are not being surpassed.
P R E P A R I N G T H E S Y S T E M B/W Thermal Medical USB Printer housing Those kinds of printers can be hosted in the lateral storage area. Procedure 1. Open the rear door. 2.
P R E P A R I N G T H E S Y S T E M 8. Switch the printer on. Always power any USB device (such as USB printers or external USB WARNING archiving devices) through the trolley. Now the system can be connected to the mains and the entire configuration can be powered through the main switch.
P R E P A R I N G T H E S Y S T E M Moving and Transporting the System Portable Configuration Disconnect all probes, peripherals and the AC/DC adapter. Close the LCD screen being sure that the safety push-buttons are closed. Always use the handle to move the system.
P R E P A R I N G T H E S Y S T E M To steadily lock the system, all the wheels must be locked. Do not park the system on a slope. Do not use the brakes to park the machine on a slope. Avoid any unnecessary mechanical shock to the system while moving it.
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P R E P A R I N G T H E S Y S T E M MyLab - G E T T I N G S T A R T E D 4 - 10...
Chapter 5. Using the System This chapter provides a brief description of the system controls. Refer to the “Advanced Operations Manual” for further detailed information. Connecting the system to the mains The power plug and the electrical main switch are located on the rear-bottom of the system.
U S I N G T H E S Y S T E M When installing , check that the power cable is not tightly bent, that MyLab WARNING it can’t be squashed by a misplaced foot or by heavy objects. Position the system in a location allowing an easy unplug of from the MyLab...
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U S I N G T H E S Y S T E M Button Description key, available on both CFM and Doppler AUTO ADJUST LEFT AUTO ADJUST modes, automatically adjusts some controls of the active mode to AN D make the echo acquisition easier.
U S I N G T H E S Y S T E M Button Description Stops the current analysis or scan and puts the system in Freeze FREEZE mode. To re-activate real time, press it again or directly press the button of the required mode.
U S I N G T H E S Y S T E M Table 5-2: Trackball cursors Mode Trackball M-Mode, Doppler LINE cursor Color Flow Mapping (CFM) CFM ROI cursor The cursor function is indicated below the image. When several cursors are present on the screen, switches between the active cursors.
U S I N G T H E S Y S T E M Pressing the button turns the system on or off, activating or closing O N /O FF the examination session. Optional Batteries When is equipped with optional batteries, the same button places the MyLab system in stand-by, partially shutting it down: in this case the initialization phase at start up is significantly reduced.
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U S I N G T H E S Y S T E M Fig. 5-1: CFM touchscreen 1. Navigation area, it contains the navigation tabs allowing to select the desired features for the relevant controls. For example B-Mode, CFM. 2.
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U S I N G T H E S Y S T E M Table 5-4: Touchscreen key status Active Key with Disabled Key Active Key Selected Key Submenu Gray text on dark White text on light As Active Key with Blue text on dark gray background gray background...
U S I N G T H E S Y S T E M Fig. 5-2: Annotations touchscreen Refer to the “Advanced Operations” manual for further details. Alphanumeric The alphanumeric keyboard is based on the QWERTY standard. The Keyboard Layout alphanumeric keys are used to enter text data in the enabled windows.
U S I N G T H E S Y S T E M Information about the Screen Layout The screen is split into four main areas. Fig. 5-3: Screen Layout 1. Heading Area 2. Footer Area 3. Image Area 4.
U S I N G T H E S Y S T E M Footer Area This area is used to display the following information: trackball functionality, Wi-Fi icon (when enabled), archival media icons, advanced features icons, ...
U S I N G T H E S Y S T E M Peripheral Devices The system is able to simultaneously manage two peripheral devices (b/w or RGB printers). The icons of the peripheral devices are shown at right of the footer area.
U S I N G T H E S Y S T E M Freeze Status Whenever an image is frozen, a memory bar is displayed (at bottom right) concerning the scrolling memories. The images acquired immediately before are frozen and archived in these memories. The trackball can be used to examine the B-Mode, M-Mode, Doppler and color information image by image.
U S I N G T H E S Y S T E M Table 5-7: Color Flow Mapping (CFM) Parameters Displayed Parameter Description format VM (Tissue Velocity nnn MHz Color frequency or T Mapping) frequency when enabled Color gain (Min,%, Max) nnn kHz Pulse Repetition Frequency Wall filter...
Chapter 6. Customizing the System can be customized to increase efficiency and streamline your work- MyLab flow. You can do the following: Create preset designed specifically for the exams you perform. Change system settings to reflect your needs. ...
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C U S T O M I Z I N G T H E S Y S T E M The menu is organized in three areas: Clinical Configuration, the upper area shows all options relating to Clinical Settings or Presets, ...
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C U S T O M I Z I N G T H E S Y S T E M System Settings System Settings define the ’s parameters related to a specific system MyLab profile: Profile Manager, DICOM configuration, ...
C U S T O M I Z I N G T H E S Y S T E M Generic Configuration Procedure Once accessed the configuration screen for the parameter you want to set, a common set of commands is available and a common setting procedure can be used.
C U S T O M I Z I N G T H E S Y S T E M Clinical Configurations This chapter explains how to set many options. For configurations not MyLab described here refer to relevant chapters in the “Advanced Operations” manual. Real Time Preset A Preset is a group of settings that optimizes the system for a specific type of exam.
C U S T O M I Z I N G T H E S Y S T E M Creating a new preset from Real-Time Procedure To create a new preset or modify an existing one: Adjust the real time image as desired in all modes (2D, CFM and Doppler).
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C U S T O M I Z I N G T H E S Y S T E M on the right the menu to record the macro and to edit the customized buttons, on the bottom the fields where customized touchscreens are named and described.
C U S T O M I Z I N G T H E S Y S T E M button adds a new tab that will be automatically displayed. Place N E W T A B the cursor on the tab and press to change its name, using the EN TER alphanumeric keyboard to edit it.
(no component has to be without any setting). Should this not solve the problem, contact Esaote personnel. Center ID Center ID allows to set the center name displayed in the Heading Area of the screen and the center information shown in the report.
C U S T O M I Z I N G T H E S Y S T E M General Setup The menu is organized in internal folders, selectable using the tabs displayed on the top of the menu. Fig.
C U S T O M I Z I N G T H E S Y S T E M Set Time Using the keyboard set the time. Time Format The time format is available on a 24 or 12 hour basis. In the 12 hour option, the time is shown as AM and PM.
C U S T O M I Z I N G T H E S Y S T E M CONTROL PANEL Folder The table below lists and explains the available fields and the corresponding actions. Table 6-3: Control Panel Folder Fields Action TRACKBALL SPEED...
If a virus is found, it is advisable to switch off the , disconnect it from MyLab the data network and call the Esaote service, which will check for the presence of a virus and restore the system. Field AVAILABLE QWERTIES...
C U S T O M I Z I N G T H E S Y S T E M Fig. 6-4: Qwerty keyboard CINE MODE Folder When set, the options AUTOMATIC PLAY TRACE AUTOMATIC PLAY respectively allow to review the stored images and the trace in cine mode when is pressed.
C U S T O M I Z I N G T H E S Y S T E M Fields Action AUTO BUTTON SETUP Sets the action after pressure: AUTOADJUST AUTO automatically adjust the B-Mode image), ECFM automatically optimize CFM image) or of them.
C U S T O M I Z I N G T H E S Y S T E M When the buttons are associated to save image or save clip, they NOTE will be named further in this manual as respectively.
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C U S T O M I Z I N G T H E S Y S T E M License Activation To activate a new license, type the license number in the field and press KEYS to confirm. If the number is correct, the status changes to V E R I F Y PERMANENT All license fields are not case sensitive with the exception of the CrystaLine...
C U S T O M I Z I N G T H E S Y S T E M Import/Export Menu The menu is organized with internal folders, selectable using the tabs displayed on the top of the menu. Fig.
C U S T O M I Z I N G T H E S Y S T E M customized SAVING OPTIONS customized center configuration ( CENTER ID customized export settings; MULTIMEDIA customized configurations; NETWORK ...
ENCRYPTION MODE Encryption Mode Encryption allows to preserve health data storage confidentiality. Encryption can be performed by Esaote Service personnel only. Encryption can be applied to the internal hard disk and to one or more external USB memory devices. At the end of encryption a recovery key will be given to you. The recovery key is stored on USB pen drive, or on file, or by printing it.
Chapter 7. Performing an Exam This chapter describes the procedures commonly used in performing patient exams with . These procedures include entering patient and application MyLab data, acquiring images, making measurements and calculations; annotating and reviewing images. Read the “Safety and Standards” manual carefully: all the safety characteristics, cautions and warnings listed there apply to all exams.
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P E R F O R M I N G A N E X A M Fig. 7-1: Patient ID screen Fig. 7-2: Probe, Application, Preset touchscreen Starting exam The steps to be followed to start an exam are: procedure 1.
P E R F O R M I N G A N E X A M Entering Patient and Application data There are two ways to enter patient data: Filling the Patient ID screen, Retrieving existing data from archive. Filling the Patient ID screen The Patient ID screen is used to enter patient data and application data, when applicable.
P E R F O R M I N G A N E X A M At any time during the exam, Patient Data can be viewed and modified by PATIENT ID pressing PATIENT ID Do not use to start a new exam of a new patient as it will update WARNING existing patient’s data with new entries.
P E R F O R M I N G A N E X A M Selecting Application When a probe has been selected, on the middle of the touchscreen all the application available with the selected probe are displayed. Tap the name of the desired application to set it.
P E R F O R M I N G A N E X A M Performing the Exam offers a set of imaging modes to cover a variety of imaging needs. By MyLab pressing the different mode buttons the specific mode is activated in real time.
P E R F O R M I N G A N E X A M Reviewing Images EXAM REVIEW During the exam, taping enables reviewing of the saved images and sequences, and the trackball automatically changes to pointer mode, allowing you to scroll through the thumbnails and select the item to be reviewed.
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P E R F O R M I N G A N E X A M At power-up, the system prompts the operator to archive the last exam NOTE performed if the system was switched off without first closing the exam in progress.
Chapter 8. System Maintenance To ensure that operates over time at its maximum efficiency, Esaote MyLab recommends to perform maintenance procedures regularly. Maintenance procedures should be performed both by the user itself and by Esaote authorized service personnel. The maintenance operations and schedule are provided in the table below.
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Periodic maintenance operations that require the access to the system can NOTE be performed only by trained personnel: contact your local Esaote representative for further information on required periodic inspections. Only trained persons are allowed to perform the safety inspection mentioned above.
S Y S T E M M A I N T E N A N C E Cleaning Operations Periodic cleaning of the system and any connected devices is important. In the event of poor maintenance, dust and dirt can compromise the reliability and performance of and connected devices.
S Y S T E M M A I N T E N A N C E Check the instructions supplied by the manufacturer of the cleaning agents for possible stricter limitation. Do not use hot cleaning agents for cleaning the equipment.
S Y S T E M M A I N T E N A N C E Invisible laser radiation. Do not view directly with optical instruments. WARNING Class 1M laser products. Do not remove the ball from the socket. Do not try to disassemble the trackball during the cleaning of the WARNING removable sealing ring.
S Y S T E M M A I N T E N A N C E Never spray or pour any liquid directly onto the screen or case. Overspray or liquid may cause electrical shock. WARNING Cleaning the LCD case Use a soft, dry cloth to wipe the surface of the case.
Licenses enable specific functions of the system, they are linked to the system serial number and are, therefore, unique. They should be carefully stored. The system is delivered by Esaote, with the licenses already installed. Additional features can be added buying the related license.
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T E C H N I C A L S P E C I F I C A T I O N S System Features Depending on the model, can be configured with one or more of the MyLab following licenses. Table 9-2: System Features Licence Feature description...
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T E C H N I C A L S P E C I F I C A T I O N S Licence Feature description Mobile application which allows to remotely review MyLab MyLab Tablet images on tablet or mobile. MyLibrary Dedicated libraries for Rheumatology, MSK, Regional anesthesia, Physiotherapy and Advanced vascular.
T E C H N I C A L S P E C I F I C A T I O N S a. Refer to www.esaote.com for further details on supported DICOM classes. b. Refer to the corresponding Sales Area manager for further information.
T E C H N I C A L S P E C I F I C A T I O N S Image Files Formats • BMP (uncompressed) • PNG (lossless) • JPEG (lossy) • AVI: Codec Microsoft MPEG-4 V2 and MS-Video 1 •...
T E C H N I C A L S P E C I F I C A T I O N S Optional batteries supplied: • up to 60’ operating autonomy (with new batteries) • standby suspension for quick startup ...
T E C H N I C A L S P E C I F I C A T I O N S Standards Table 9-3: Standards Standard Title IEC 60601-1:2012 (Ed.3.1) Medical electrical equipment - Part 1: General EN 60601-1:2006 + CORR. 1 requirements for basic safety and essential (2006) + CORR.
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T E C H N I C A L S P E C I F I C A T I O N S Standard Title AIUM/NEMA UD-3:2004 Standard for Real Time Display of Thermal and (R2009) Mechanical Acoustic Output Indices on Diagnostic Ultrasound Equipment.
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