User's Guide

Symbol Glossary
Symbol Definition
CE mark
Single Use. Do not re-use.
Follow Instructions for Use
WEEE Symbol
Manufacturer
Date of Manufacture YYYY MM DD
Defibrillation-proof type BF applied part.
The entire CPRcard is the applied part.
Warning/Caution
Device catalogue number reference
Unique Device Identification
Ingress protection rating
Temperature limitations
Humidity limitations
Pressure limitations
Machine readable Unique Device Identification (UDI).
Datamatrix with UDI numbers (XXX = last three UDI digits)
Not to be used in a bed or on soft surfaces
Not for patient under 8 years
UDI
CPRcard
User Guide
EN
www.laerdal.com
Specifi cations
Dimensions Height 86 mm x Width 54 mm x Depth 2 mm
Weight < 7 g
External Material Polycarbonate (PC) and self-adhesive medical tape.
Battery Non-rechargeable lithium battery 15 mAh nominal
capacity*
Typical battery life: >30 minutes of CPR
End-of-shelf-life battery life: minimum 10 minutes
of CPR
Shelf life 3 years from the production date
Operating/Storage
Conditions
Temperature: 0 – 40 °C (32 – 104 °F)
Humidity: ≤ 90% RH
Atmospheric Pressure: 620 – 1060 hPa
Shipping Conditions Temperature: -40 – 40 °C (-40 – 104 °F)
Humidity: ≤ 90% RH
Atmospheric Pressure: 550 – 1060 hPa
Bluetooth® Low
energy transmitter
Frequency band: 2.400 – 2.4835 GHz
Modulation: Gaussian frequency shift modulation
Maximum radio-frequency shift modulation: 1 mW
Effective radiated power: 0 dBm
Ingress protection
rating
IP67. Dust tight, and protected against water
submersion to 1 meter (3.3 feet) for 30 minutes
*Battery performance varies with temperature.
Caution
Do not store your CPRcard above 40 °C as this may reduce the lifetime of the battery.
Electromagnetic Conformity
The device is intended for use outdoors and indoors except for near HF surgical
equipment, and the RF shielded room for magnetic resonance imaging.
No particular actions are required to maintain safety and performance with regard
to electromagnetic disturbances for the expected service life.
Warnings
• Use of this equipment adjacent to or stacked with other equipment should be
avoided because it could result in improper operation. If such use is necessary, this
equipment and the other equipment should be observed to verify that they are
operating normally.
• Portable RF communications equipment (including peripherals such as antenna
cables and external antennas) should be used no closer than 30 cm (12 in) to any
part of the CPRcard. Otherwise, degradation of the performance of this equipment
could result.
Electromagnetic Emissions Tests
Emissions Test Standard or test
method
Compliance
RF emissions CISPR 11 Group 1 Class B Group 1 Class B
Harmonic emissions IEC 61000-3-2 Class A
Voltage fluctuations/ flicker
emissions
IEC 61000-3-3 Complies
Electromagnetic Immunity Tests
Immunity Test Standard or test
method
Compliance Level and
Immunity Test Level
Electrostatic discharge IEC 61000-4-2 ±8 kV contact
±2kV, ±4kV, ±8kV
±15 kV air
Radiated RF EM fields IEC 61000-4-3 10 V/m
80 MHz – 2.7 GHz
80% AM at 2 Hz
Proximity fields from RF
wireless communication
equipment
IEC 61000-4-3 380-390 MHz: 27 V/m
430-470 MHz: 28 V/m
704-787 MHz: 9 V/m
800-960 MHz: 28 V/m
1700-1990 MHz: 28 V/m
2400-2470 MHz: 28 V/m
5100-5800 MHz: 29 V/m
Rated power frequency IEC 61000-4-8 30 A/m
50 Hz or 60 Hz
Electrical fat transients
/ bursts
IEC 61000-4-4 ±2 kV
100 kHz repetition frequency
Surges: Line-to-line IEC 61000-4-5 ±0.5 kV. ±1 kV
Surges: Line-to-ground IEC 61000-4-5 ±0.5 kV. ±1 kV. ±2 kV
Conducted disturbances
induced by RF fields
IEC 61000-4-6 3 V ; 0.15 MHz – 80 MHz
6 V in ISM and amateur radio
bands between 0.15 MHz
and 80 MHz
80% AM at 1 kHz
Voltage dips IEC 61000-4-11 0% U
T
; 0.5 cycle
At 0°, 45°, 90°, 135°, 180°,
225°, 270° and 315°
0% U
T
; 1 cycle and 70% U
T
;
25/30 cycles
Single phase: at 0°
Voltage interruptions IEC 61000-4-11 0% U
T
; 250/300 cycle
U
T
is the a.c. mains voltage prior to application of the test level.
20-18063 Rev A
Support
If you need assistance or to report any issues, contact a local Laerdal representative
or visit www.laerdal.com/CPRcard for more information.
Waste Handling
WEEE
This appliance is marked according to the European directive 2012/19/EU on
Waste Electrical and Electronic Equipment (WEEE).
By ensuring this product is disposed of correctly, you will help prevent potential
negative consequences for the environment and human health, which could
otherwise be caused by inappropriate waste handling of this product.
The symbol on the product indicates that this appliance may not be treated as
household waste. Instead, it shall be handed over to the applicable collection point
for the recycling of electrical and electronic equipment.
Disposal must be carried out in accordance with local environmental regulations
for waste disposal.
Caution
Do not cut the device as this may damage the battery and expose harmful chemicals.
Service and Warranty
CPRcard does not have any replaceable or serviceable parts.
The CPRcard has a one-year limited warranty. Refer to the Laerdal Medical
Warranty for terms and conditions.
For more information visit www.laerdal.com.
Federal Communications Commission (FCC) and Industry Canada
(IC) Statements
This device complies with part 15 of the FCC Rules and Industry Canada’s
licence-exempt RSSs. Operation is subject to the following two conditions:
1. This device may not cause harmful interference, and
2. This device must accept any interference received, including interference that may
cause undesired operation.
Le présent appareil est conforme aux CNR d’Industrie Canada applicables
aux appareils radio exempts de licence. L’exploitation est autorisée aux deux
conditions suivantes:
1. L’appareil ne doit pas produire de brouillage, et
2. L’appareil doit accepter tout brouillage radioélectrique subi, même si le brouillage
est susceptible d’en compromettre le fonctionnement.
Caution
Changes or modifications not expressly approved by Laerdal Medical could void the
user’s authority to operate the equipment.
FCC ID: QHQ-20-10468
IC: 20263-2010468
This product is in compliance with the essential requirements of EU Council
directive 93/42/ EEC as amended by EU Council directive 2007/EC, Council
Directive 2014/53/EU on Radio Equipment (RED) and Council Directive 2011/65/
EU on restriction of the use of certain hazardous substances (RoHS).
www.laerdal.com
Laerdal® and CPRcard (logo)® and CPRcard™ are trademarks of
Laerdal Medical AS. Ownership and all rights reserved.
© 2021 Laerdal Medical AS. All rights reserved.
Manufactured in China for:
Laerdal Medical AS,
P.O. Box 377
Tanke Svilandsgate 30,
4002 Stavanger, Norway
Printed in China
www.laerdal.com/CPRcard
Specifi cations
Compression
Depth
Depth feedback is based on the median depth of the
last 5 compressions.
Compressions with a depth of less than 1 cm or more
than 10 cm will not be detected
Compression depth
accuracy
±5 mm or ±10%, whichever is greater
Compression Rate Rate feedback is based on the median rate of the last
5 compressions.
Compression rate
accuracy
±5%
< 5 cm (2.0 in)
5 – 6 cm (2 – 2.36 in)
> 6 cm (2.36 in)
< 100 /min
100 – 120 /min
> 120 /min
Troubleshooting
Symptom Possible cause Possible solution
Card does not
turn on (no LEDs
turning on)
• On/Off button is not
sufficiently pressed
• Card temperature is
below 0 °C (32 °F)
• The device is broken
• Press and hold the On/
Off button firmly to try
to turn on the CPRcard.
• If the problem persists,
do not use the CPRcard
on a patient.
Warning LED
turns on at
start-up and stays
on for 1 minute
• Internal error detected
• Depleted battery
• Turn the card off and
on again.
• If the problem persists,
do not use the CPRcard
on a patient.
Not all LEDs light
up at start-up
The device is broken.
CPRcard turns off
during CPR
• Compression inactivity
> 1 min
• Accidental activation of
On/Off button
• Internal error detected.
• Depleted battery
Do not interrupt CPR –
continue CPR without
feedback.
Depth target
(green LED) not
achieved during
CPR
• Too shallow
compressions
• Incomplete release
(leaning)
Press harder and release
completely between
compressions.
The CPRcard
moves around
during CPR
The liner was not removed
before the CPRcard was
placed on the patient.
Remove the liner and
place the CPRcard on
the patient’s bare chest as
quickly as possible to avoid
interrupting CPR.
Inactivity
indication while
performing
compressions
• Chest compressions not
detected
• Too shallow
compressions (<1 cm)
• Too slow compressions
(<40/min)
Press harder and/or
faster. Release completely
between compressions.
Bluetooth
connectivity issues
Do not interrupt CPR –
continue CPR.
Get Familiar with CPRcard
CPR is best performed by CPR-trained rescuers. It is also recommended
to get familiar with the CPRcard by practicing on a training manikin using
standard CPR technique.
Practice following the feedback from the CPRcard:
1. Turn on CPRcard.
2. Place the card correctly without removing the liner from the
adhesive. (See Correct Placement on page 6).
3. Focus on depth feedback (See Compression Depth on page 8).
Gradually increase the depth of compression so that the
recommended depth target is reached.
4. Focus on rate feedback (see Compression Rate on page 8).
Compress slowly and gradually increase the rate of compression until
each of the rate indicators lights up.
5. Focus on performing compressions at an adequate depth and rate.
6. Remember to release between each compression.
To stay familiar with the CPRcard, repeat as often as needed.
Caution
Do not practice on a person as this may cause injuries to the person.
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