CAE Luna User manual

Your worldwide
training partner
of choice
User Guide

Proprietary Notice
This document, including the information contained herein, is condential and/or proprietary to CAE Inc., and shall not be
reproduced or disclosed in whole or in part, or used for any purpose whatsoever without the prior written authorization of CAE Inc.
Trademark Information
Trademarks and/or registered trademarks of CAE Healthcare Inc. and/or its aliates include but are not limited to: Apollo,
Ares, AresAR, Aria, Athena, BabySIM, BluePhantom, Caesar, CathLabVR, EndoVR, HPS, ICCU, InfantSIM, iStan, Juno, LapVR,
LearningSpace, Lucina, LucinaAR, Luna, Maestro, Medicor, METIman, Müse, NeuroVR, PediaSIM, SimEquip, Simulex, StethoSym,
SymDefib, SymEyes, UniSIM, Vimedix, VimedixAR and Vivo. All other brands and product names are trademarks or registered
trademarks of their respective owners. All logos, tradenames and trademarks referred to and used herein remain the property
of their respective owners and may not be used, changed, copied, altered, or quoted without the written consent of the
respective owner. All rights reserved.
CAE ©2022

©2022 CAE 905K560252 v1.2 i
Contents
CONTENTS
Cautions and Warnings .............................................................................................. 1
Electrical Safety. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Product Use Warnings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Manikin. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Fluids System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2
Simulator Batteries. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
Battery Replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Battery Safety Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Precautions for Handling. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Potential Health Effects . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Safety Measures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Transport Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
System Requirements ................................................................................................ 7
Software and Hardware . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
CAEMaestro Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Windows® Operating System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7
Approved Devices . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Specifications .............................................................................................................. 9
Size and Weight . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Ambient Temperature Range. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Maximum Altitude . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9
Power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10
Communications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10
Electrotherapy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10
Meet Luna.................................................................................................................. 11
Simulator Configurations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .12
Equipment Overview................................................................................................ 15
Standard Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .15
Male and Female Genitalia . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .16
Live and Advanced Configurations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .17
Canvas Rolling Bag . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18
Surface Go Tablet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .18

Contents
ii ©2022 CAE 905K560252 v1.2
CAELuna
Tablet Carrying Case . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .19
CAE StethoSym . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .19
CAE SymDefib . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .19
Optional Equipment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .20
Patient Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .20
Setup Preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .21
Unpacking the Manikin . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .21
Setup Steps . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .22
Step 1: Place Luna in Work Area. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .22
Step 2: Configure the Wired Connection. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .22
Step 3: Power on the Manikin. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .24
Step 4: Set up the Wireless Network . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .24
Step 5: Power on the Instructor Workstation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .25
Step 6: Launch Maestro . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .26
Step 7: Set up TouchPro Monitor (Optional). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .26
Step 8: Charge the StethoSym . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .26
Step 9: Prime the Fluid Systems (Optional). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .27
Luna Features............................................................................................................ 31
Neonatal Manikin. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .31
Physiological and Pharmacological Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .31
Cardiovascular System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .31
Respiratory System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .33
Neurologic System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .34
Genitourinary System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .34
Articulation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .35
Medication Administration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .35
Simulated Clinical Experiences. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .36
Scenarios . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .37
System Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .37
Application Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .37
System Tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .37
Using Luna ................................................................................................................. 39
Cardiovascular System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .40
Cardiovascular System Controls. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .40
Pulses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .41
Peripheral Intravenous (IV) Sites . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .41

©2022 CAE 905K560252 v1.2 iii
Contents
Central Intravenous (IV) Sites . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .42
Arterial Sites . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .42
Intramuscular (IM)/Subcutaneous (SQ) Sites . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .43
Intraosseous (IO) Site . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .43
Heart Rate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .44
Chest Compressions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .44
ECG . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .44
Defibrillation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .45
Respiratory System. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .48
Respiratory System Controls. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .48
Airway Management . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .49
Intubation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .50
Laryngospasm. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .51
Bag Valve Mask (BVM) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .51
Needle Decompression . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .52
Chest Tube. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .53
Cyanosis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .53
Tracheostomy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .54
Neurologic System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .55
Neurologic System Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .55
Eyes. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .56
Intracranial Pressure (Fontanel) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .57
Genitourinary System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .57
Changing the Simulator’s Genitalia . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .57
Urinary Catheterization . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .58
Medication Administration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .58
Administration via Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .58
Intravenous, Intramuscular/Subcutaneous, and Intraosseous Medication. . . . . . . . . .59
Fluids . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .59
Sounds . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .59
Vocal Soundsh. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .60
Using the StethoSym . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .60
Umbilical Cord. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .63
Care and Maintenance ............................................................................................. 65
General Simulator Care. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .65
Storage. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .65

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Short-Term Storage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .66
Long-Term Storage. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .66
Breakdown . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .67
Step 1: Clean the Manikin . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .67
Step 2: Remove Excess Fluids . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .67
Step 3: Power off the Instructor Workstation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .69
Step 4: Power off the Manikin. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .70
Appendix A -Recommended Clinical Supplies ....................................................... 71

©2022 CAE 905K560252 v1.2 1
Cautions and Warnings
CAUTIONS AND WARNINGS
It is important to read and understand these cautions and warnings before you use the Product.
Electrical Safety
Important: Do not use the product in any manner other than specified, as safety features designed
for protection may be impaired.
• This product must be connected to an electrical outlet that is properly grounded. Take
precaution to ground or polarize correctly.
• Connect only to a 100-240 VAC 50/60Hz power source.
• Always use the supplied power cords. Do not substitute.
• Always use the supplied power adapter to run the simulator from AC.
• Do not allow excess fluids to flow on or into electronic parts.
• Do not attempt to disassemble the simulator or service any of the electrical components
without receiving instructions from Customer Service.
• Do not operate the manikin in rain. Apply water to the manikin only in accordance with the
supported clinical procedures explained in this guide.
Product Use Warnings
Manikin
• Make sure the manikin is set up on a stable, sturdy work surface that will not collapse and
cause injury to users.
• Operate the manikin in ambient temperatures below 104°F (40°C).
Note: This only applies when using the manikin without the tablet where CAEMaestro
software is installed. For information about temperature ranges for the tablet, see
Ambient Temperature Range in the Specifications section of this User Guide.
• Do not place foreign substances into the airway, with the exception of small amounts of
approved lubricant. Only perform invasive procedures supported by the Product as
described in the applicable sections of the User Guide.
• Do not insert any materials into the manikin except the equipment or probes supplied.
• Do not lift the manikin by its limbs. Support the head and lift it from the torso. If necessary,
have another person help you lift and move the manikin using a patient transfer device
such as a patient transfer board, when available.
• Keep the manikin plugged in between training sessions due to a slow drain of the battery
that occurs.

Cautions and Warnings
2 ©2022 CAE 905K560252 v1.2
CAELuna
• Under normal circumstances, unplugging the external DC power used for powering and
charging the manikin is not necessary because the charging stops when the battery is full.
A topping charge is only applied when the battery voltage drops to a certain level.
• Do not spill fluids over the manikin’s chest, abdomen, or inside the manikin’s torso. This
could damage the system and may also present a possible hazard for the operator.
Special attention should be taken while using the the various fluid features.
• Do not use the manikin or equipment in locations where children are likely to be present.
Fluids System
For manikins such as Luna that are equipped with fluid systems:
• Do not modify the reservoirs or any assembly component.
• Always protect your eyes, skin, and clothing against accidental exposure.
Battery
Manikins and tablets use lithium batteries that all have special handling requirements to avoid
hazardous situations.
For more information about battery specifications, see the Specifications section. For more
information about battery safety, see the Battery Safety Information section.
Simulator Batteries
• Always store the polymer lithium-ion battery pack indoors.
• Always keep the battery away from objects or materials with static electric charges.
• Batteries can be charged while the manikin is between 32°F (0°C) and 113°F (45°C).
• Do not store, use or charge the battery inside of an automobile as
temperatures can exceed 176°F (80°C).
Manufacturer RRC power solutions GmbH
Technologiepark 1, D-66424 Homburg-Saar, Germany
Mail: [email protected]
Emergency phone
number
[phone] (8.00 – 16.00, MEZ), or contact your national poison
information center.

©2022 CAE 905K560252 v1.2 3
Cautions and Warnings
Battery Replacement
• If the simulator battery power diminishes significantly, contact Customer Service to
replace the battery. For safety, only replace the battery with an approved make and
model.
• Before disposing of a simulator battery, apply vinyl tape to its positive (+) and negative (-)
terminals to avoid short circuits.
• If a simulator battery needs to be replaced, immediately remove the old battery from the
equipment to ensure no damage occurs.
• Do not dispose of the simulator battery into a fire. Dispose of or recycle
batteries responsibly.
Battery Safety Information
For information about battery specifications, see the Specifications section of this user guide.
Important: Refer to the battery manufacturer’s Safety Data Sheet (SDS) for complete safety
instructions and handling information.
Precautions for Handling
Hazards are associated with the contents of the cell or battery. Under recommended use conditions,
the electrode materials and liquid electrolyte are non-reactive, as long as the cell or battery integrity
remains, and the seals remain intact.
Potential exposure should not exist unless the cell or battery:
• leaks,
• is exposed to high temperatures,
• is mechanically, electrically or physically abused/damaged.
If the cell or battery is compromised and starts to leak, based upon the battery ingredients, the
contents are classified as hazardous. In general, if liquid leaks from the battery or foul odor is
detected, DO NOT use the battery and keep it away from heat or flame.
• Avoid short circuiting the battery. Do not store with coins, screws or other similar objects.
• Do not immerse in water.
• Do not disassemble or deform the battery.
• Do not expose to, or dispose of the battery in fire.
• Avoid excessive physical shock or vibration.
• Keep out of the reach of children.

Cautions and Warnings
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• For rechargeable batteries, the battery must be charged in an approved charger.
• Never use a modified or damaged charger.
• Store in a cool, dry, and well-ventilated area.
• Never use a battery that has been damaged or deformed.
• Do not short-circuit the positive (+) and negative (-) terminals.
• Do not place the battery in a device with the positive (+) and negative (-) terminals in the
wrong positions.
• Do not solder a battery directly.
Potential Health Effects
• Acute (short term): In the event that the cell or pack ruptures, the electrolyte solution
contained within the cell will corrode and can cause burns to skin and eyes.
• Inhalation: Inhaling materials from a sealed cell is not an expected route of exposure.
Vapors or mists from a ruptured cell can cause respiratory irritation.
• Ingestion: Swallowing materials from a sealed cell is not an expected route of exposure.
Swallowing the contents of an open cell can cause serious chemical burns to mouth,
esophagus, and gastrointestinal tract.
• Skin: Contact between the cell and skin will not cause any harm. Skin contact with the
contents of an open cell can cause severe irritation or burns to the skin.
• Eye: Contact between the cell and the eye will not cause any harm. Eye contact with the
contents of an open cell can cause severe irritation or burns to the eye.
• Interactions with other chemicals: Immersion in high conductivity liquids
can corrode or breach the cell or battery enclosure. The electrolyte
solution inside of the cells can react with alkaline (basic) materials and
present a flammability hazard.
Safety Measures
Review the precautions for handling before replacing a battery utilizing guidance from CAE.
Should exposure to hazardous battery components occur, or in the event of a fire, follow all local first
aid measures and safety protocols.
Transport Information
CAE complies with the most current International Air Transport Association (IATA) Dangerous Goods
Regulations when transporting and shipping Li-ion batteries. The following terms are defined as
follows:

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Cautions and Warnings
Consignment - Equivalent to the term "shipment,” meaning one or more packages of
hazardous materials accepted from one shipper at one time and at one address, receipted
in one lot, and moving to one consignee at one destination address.
Equipment - The device or apparatus for which the lithium cells or batteries will provide
electrical power for its operation.
It is the shipper’s responsibility to ensure that the consignment is packed in compliance to the latest
edition of the applicable regulations. Regulations require appropriate training for shipping dangerous
goods. Shipping regulations and requirements may vary depending upon:
• Wattage of the battery.
• Whether the battery is shipped independent of, contained within, or packed
with the equipment.
When transporting batteries CAE follows these documentation and labeling requirements:
Item Description
Batteries Shipped Independent of
the Manikin, Tablet, and Laptop
Batteries contained in or packed
with the Manikin, StethoSym,
Tablet, Laptop, and HoloLens
UN No. 3480N No. 33480480 3481
UN Shipping
Name:
Lithium-ion Batteries Lithium-ion Batteries
Transport Hazard
Class:
9 9
Labeling:

Cautions and Warnings
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System Requirements
SYSTEM REQUIREMENTS
This section describes the minimum and optimal requirements to run the simulator.
Software and Hardware
Any computer (or tablet) used to operate the Maestro or Patient Monitor software must meet
hardware and software requirements. However, optimal requirements should be met to enhance
performance. These requirements also apply to devices running Maestro Standalone.
CAEMaestro Software
The following identifies the software version associated with the release of this user guide.
Note: There are periodic system updates for Maestro that can be downloaded from any device with
an Internet connection. The updates are available at: https://www.caehealthcare.com/support/
software-updates/
Windows® Operating System
Document Document Version Software Version
Maestro for Luna 905K560452 v1.2 CAE Maestro v1.8
Luna User Guide 905K600252 v1.1 CAE Maestro v1.8
Minimum Requirements
Software • Win 10 Pro
• .NET 4.8
Hardware • Surface Go 2
• Intel Pentium Gold Processor 4425Y
• 4 GB DDR3 RAM
• 32 GB Hard Drive space available
• 1920x1280 screen resolution
• USB-C
• Wireless 802.11 a/b/g/n/ac/ax

System Requirements
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Approved Devices
Note: Upon installation, the software takes up 1.2 GB of hard drive space. For standalone versions of
Maestro, the software can store approximately 30.8 GB of patient record files. If this storage capacity
is expected to be maximized, plan for additional hard drive space.
Make/Model • Microsoft Surface Go
Software • Windows 10
• Chrome version 62 or higher (not required for use with Maestro v1.8 or
later)
Hardware • Intel Core 2 Duo, 2.0 GHz
• 8 GB DDR3 RAM
• 32 GB Hard Drive space available
• 1366x768 screen resolution
• USB-C Port
• Wireless 802.11b/g/n Ethernet card 100BASE-T Ethernet Adapter

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Specifications
SPECIFICATIONS
All hardware and software needed for operating the simulator are provided with the shipment.
Size and Weight
Ambient Temperature Range
Maximum Altitude
Battery
Equipment Size Weight
Manikin/Simulator 21” H (53.34 cm) 8 lbs (3.63 kg)
SymDefib 2.6” H x 4.9” W x 5” D
(6.6 cm x x 12.4 cm x 12.7 cm)
8 oz (227 g)
Item Operation Storage Relative Humidity
Manikin/Simulator 40°F to 104°F
(4°C to 40°C)
40°F to 122°F
(4°C to 50°C)
0% to 90%
non-condensing
Tablet 50°F to 95°F
(10°C to 35°C)
-13°F to 113°F
(-24°C to 45°C)
0% to 90%
non-condensing
SymDefib 0°C- 35°C
Note: Indoor use only
-20°C – 60°C 45% to 85%
Item Operation Storage Shipping
Tablet 10,000 ft (3,048 m) 15,000 ft (4,572 m) 35,000 ft (10,668 m)
Item Description
Commercial product name RRC1130
Use of the substance/
preparation
Lithium-ion (Li-ion) battery
Additional Information Battery-System: Lithium-ion
Wh rating: 14.7 Wh
SymDefib Battery Li-ion 3.7V 2200mAh

Specifications
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Power
Communications
Electrotherapy
Item Description
Power Adapter • AC Input: AC 100-240 VAC, 50/60 Hz
Manikin/Simulator • Internal Batteries: Rechargeable
• Run Time: 4 hours (typical)
StethoSym • Run Time: 2 hr 45 min while constantly reading a RFID tag and
playing audio; 4 hours when ON and receiving signal (Sleep
Mode)
• Recharge time: 50 minutes
SymDefib • AC input: 100-240VAC 50/60Hz
• Nominal DC Output: 5 V
• Maximum DC Current Output: 4 A
• Nominal Power: 20 W
• Run Time: 17 hours (with Pads not on manikin),
2-3 hours (with Pads on manikin)
Item Description
Simulator Network • IEEE 802.15.4
Item Description
Defibrillation • 20 to 200 Joules (Monophasic, Biphasic)
Pacing • 20 mA to 180 mA

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Meet Luna
MEET LUNA
Luna is the youngest member of CAE Healthcare’s family of patient simulators. This neonate
simulator allows learners to practice interventions, procedures and treatments at different stages of
development through simulated clinical scenarios. The live and advanced configurations of the
simulator incorporate infant patient physiological models that generate realistic and automatic
responses to clinical interventions and medication administrations that are specific to neonatal
patients.
Luna

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Simulator Configurations
The simulator is available in three configurations.
Configuration Components
Base • Interchangeable gender
• Bleeding via externally connected IV
• Anatomically correct airway
• Intubation: oral and nasal endotracheal, right mainstem
• Laryngeal mask placement
• Airway insertion: oropharyngeal and nasopharyngeal
• Suctioning: oral and nasopharyngeal (procedural only)
• Pre-made tracheostomy site
• Manual chest excursion via bag-valve-mask, endotracheal
tube, and tracheostomy
• Asymmetrical chest excursion with right mainstem intubation
• Chest compressions
• Intraosseous (IO) access site
• Intramuscular (IM) injections
• Peripheral venous access (3 sites)
• Subcutaneous (SQ) injections
• Peripheral arterial catheter placement
• Subclavian catheter placement
• Articulated limbs, jaw, and neck
• Removable umbilical cord and supporting cut-down
• Manual tristate eyes
• Manual adjustable fontanel
• Feeding tube placement
• Gastric distention with esophageal intubation
• Urinary catheterization with fluid return
Live • Base features
• Instructor tablet
• Internal battery
• Wireless facilitator control
• Facilitator controlled CAE Maestro software
• Emulated patient monitor software
• Sounds: heart, lung, bowel, vocal
• Bilateral brachial pulses
• Variable pulse strength
• Library of cardiac rhythms
• Chest compression metrics
• Chest tube placement
• Pneumothorax decompression
• Commercial ECG device compatible

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Meet Luna
Advanced • Live features
• Laryngospasm
• Spontaneous breathing
• Variable respiratory and breathing patterns
• Simulated defibrillator (SymDefib)
• Pneumothorax decompression detection
• Substernal retractions
• Pulses: bilateral femoral and umbilical
• Circumoral cyanosis
• Active arm movement
Optional Components • Physiological model
• Commercial defibrillator compatible
• External lung
Configuration Components

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