laerdal Little Anne User manual

Little Anne
Important Product Information
EN

2 3
English
Little Anne
This Important Product Information covers Little Anne,
Little Anne AED and Little Anne QCPR.
Unless otherwise specified the information applies to
all product configurations.
Warnings and Cautions
A Warning states a condition, hazard, or unsafe practice
that can result in serious personal injury or death.
A Caution states a condition, hazard, or unsafe practice
that can result in minor personal injury or damage to
the manikin.
Care, Maintenance and Cleaning
Keep the manikin clean and in a hygienic condition.
Replace the airway assembly after every class, especially
if mouth to mouth resuscitation is practiced.
We recommend that you use a separate Laerdal
Manikin Face for every student.
If several students use one manikin face, thoroughly
sanitize the manikin face after every use.
Clean all skin parts regularly. Use warm soapy water or
Laerdal manikin wipes.
Use of Manikin Face Shields provides a clean barrier
between your lips and the manikin face.
These can discolor the manikin:
Pigments from lipstick and pens
Latex gloves
Using clothes other than Little Anne clothing.
Symbol Glossary
Manufacturer
Date of Manufacture
Reference Order Number
LOT Number

Operating
temperature
5 °C to 35 °C
(41 °F to 95 °F)
Degradation in product
performance may be experienced
when used at low temperatures
(below 15 °C / 59 °F)
Storage
temperature
-10 °C to 50 °C
(14 °F to 122 °F)
Humidity 5 % - 95 % relative humidity
Weight 4.2 kg (+/- 200 g)
Dimensions 65 cm x 34 cm x 21 cm
(25.6” x 13.4” x 8.3”)
Warranty
Refer to the Laerdal Global Warranty for terms and
conditions. For more information visit www.laerdal.com

3
English
Little Anne AED
Cleaning
Do not use liquids to clean inside the manikin.
Do not submerge any parts.
Battery
Only use consumer grade, non-rechargeable, carbon
zinc or alkaline batteries, 9V 6LR61. Batteries must
be replaced with correct type. Remove batteries if
product is not to be used for an extended period.
Federal Communications Commission
Statement and Industry Canada Statements
This device complies with part 15 of the FCC rules.
Operation is subject to the following two conditions:
1. This device may not cause harmful interference
2. This device must accept any interference received,
including interference that may cause undesired
operation.
Caution
Changes or modifications not expressly approved by
Laerdal Medical could void the user’s authority to operate
the equipment.
This equipment has been tested and found to comply
with the limits for a Class B digital device, pursuant to
part 15 of the FCC Rules. These limits are designed
to provide reasonable protection against harmful
interference in a residential installation. This equipment
generates, uses and can radiate radio frequency energy
and, if not installed and used in accordance with the
instructions, may cause harmful interference to radio
communications. However, there is no guarantee that
interference will not occur in a particular installation.
If this equipment does cause harmful interference to
radio or television reception, which can be determined
by turning the equipment off and on, the user is
encouraged to try to correct the interference by one
or more of the following measures:
• Reorient or relocate the receiving antenna.
• Increase the separation between the equipment
and receiver.
• Connect the equipment into an outlet on a
circuit different from that to which the receiver
is connected.
• Consult the dealer or an experienced radio/TV
technician for help.
Symbol Glossary
Little Anne AED
This product is in compliance
with the essential requirements of
Council Directive 2014/30/EU on
electromagnetic compatibility (EMC)
and Council Directive 2011/65/EU
on Restriction on the use of certain
hazardous substance (RoHS)
Australian Radiocommunications and
EMC Compliance Mark
Dispose of in accordance with your
country’s recommendations
FCC Declaration of Conformity label
KC (Korea Certification)
certification mark
Waste Handling
The Little Anne AED Sensor contains electronic
components. Dispose of it at the applicable recycling
facility in accordance with local regulations.
European directive 2012/19/EU (WEEE)
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, or on the documents
accompanying 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 electrial and electronic equipment.
Disposal must be carried out in accordance with local
environmental regulations for waste disposal. For more
detailed information about treatment, recovery and
recycling of this product, please contact your local
city office, your household waste disposal service or
the Laerdal representative where you purchased the
product.

4
English
Little Anne QCPR
Cleaning
Do not use liquids to clean inside the manikin.
Do not submerge any parts.
Battery
Only use consumer grade, non-rechargeable, carbon
zinc or alkaline batteries, LR6 1.5V AA. Batteries must
be replaced with correct type. Remove batteries if
product is not to be used for an extended period.
Federal Communications Commission
Statement and Industry Canada Statements
This device complies with part 15 of the FCC rules.
Operation is subject to the following two conditions:
1. This device may not cause harmful interference
2. This device must accept any interference received,
including interference that may cause undesired
operation.
Caution
Changes or modifications not expressly approved by
Laerdal Medical could void the user’s authority to operate
the equipment.
This equipment has been tested and found to comply
with the limits for a Class B digital device, pursuant to
part 15 of the FCC Rules. These limits are designed
to provide reasonable protection against harmful
interference in a residential installation. This equipment
generates, uses and can radiate radio frequency energy
and, if not installed and used in accordance with the
instructions, may cause harmful interference to radio
communications. However, there is no guarantee that
interference will not occur in a particular installation.
If this equipment does cause harmful interference to
radio or television reception, which can be determined
by turning the equipment off and on, the user is
encouraged to try to correct the interference by one
or more of the following measures:
• Reorient or relocate the receiving antenna.
• Increase the separation between the equipment
and receiver.
• Connect the equipment into an outlet on a
circuit different from that to which the receiver
is connected.
• Consult the dealer or an experienced radio/TV
technician for help.
Little Anne QCPR
Contains FCC ID: QHQ-120-60750
IC: 20263-12060750

MSIP-CMM-Lm1-120-60750
Symbol Glossary
Little Anne QCPR
This product is in compliance with
the essential requirements of Council
Directive 2014/53/EU on Radio
Equipment (RED), and Council
Directive 2011/65/EU on Restriction on
the use of certain hazardous substance
(RoHS).
Australian Radiocommunications and
EMC Compliance Mark
Dispose of in accordance with your
country’s recommendations
FCC Declaration of Conformity label
KC (Korea Certification)
certification mark
Do not touch
Waste Handling
The Little Anne QCPR Sensor contains electronic
components. Dispose of it at the applicable recycling
facility in accordance with local regulations.
European directive 2012/19/EU (WEEE)
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, or on the documents
accompanying 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 electrial and electronic equipment.
Disposal must be carried out in accordance with local
environmental regulations for waste disposal. For more
detailed information about treatment, recovery and
recycling of this product, please contact your local
city office, your household waste disposal service or
the Laerdal representative where you purchased the
product.

20-11796 Rev B
www.laerdal.com
© 2017 Laerdal Medical AS. All rights reserved.
Manufactured in China for:
Laerdal Medical AS
P.O. Box 377
Tanke Svilandsgate 30, 4002 Stavanger, Norway
T: ([phone]
Printed in China