Little Baby QCPR
Important Product Information
重要产品信息
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www.laerdal.com
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English
Little Baby QCPR
This Important Product Information covers Little
Baby 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 product.
Notes
A note states important information about the
product or its operation.
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 what comes with
the product originally.
Cautions
• 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.
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Federal Communications Commission
(FCC) and Industry Canada (IC) State-
ments
This device complies with part 15 of the FCC
Rules and RSS-210 of IC rules. 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.
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.
• Consult the dealer or an experienced radio/TV
technician for help.
Caution: Changes or modifications not expressly
approved by Laerdal Medical could void the user’s
authority to operate the equipment.
The term “IC” before the equipment certification
number only signifies that the Industry Canada
technical specifications
were met.
Mise en garde: Tout changement ou toute
modification n’ayant pas fait l’objet d’une
approbation expresse de Laerdal Medical peut
annuler le droit dont dispose l’utilisateur de se
servir de l’équipement.
Le terme « IC » qui précède le numéro d’agrément
de l’équipement signifie uniquement que les
caractéristiques techniques spécifiées par Industrie
Canada sont respectées.
This device contains licence-exempt transmitter(s)/
receiver(s) that comply with Innovation, Science
and Economic Development Canada’s licence-
exempt RSS(s). Operation is subject to the
following two conditions:
1. This device may not cause interference.
2. This device must accept any interference,
including interference that may cause undesired
operation of the device.
L’émetteur/récepteur exempt de licence contenu
dans le présent appareil est conforme aux
CNR d’Innovation, Sciences et Développement
économique 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;
2. L’appareil doit accepter tout brouillage
radioélectrique subi, même si le brouillage
est susceptible d’en compromettre le
fonctionnement.
Little Baby QCPR contains FCC ID:
QHQ-QCPR-LB
Contains IC Certification Number:
20263-QCPRLB
Canada
This Class B digital apparatus complies with
Canadian ICES-003.
Japan
MIC certification 012-190010
Korea
R-C-Lm1-QCPR-LB
China
CMIIT ID: 2019DJ12628
English
Little Baby QCPR
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English
Little Baby QCPR
EU
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).
UK
UKCA (U.K. Conformity Assessed): This product
complies with the requirements of U.K. legislation
of Radio Equipment Regulations (S.I. 2017/1206).
UKCA (U.K. Conformity Assessed): This product
complies with the requirements of U.K. legislation
of Restriction of the Use of Certain Hazardous
Substances in Electrical and Electronic Equipment
Regulations (RoHS) Regulations((S.I. 2012/3032).
Waste Handling
The QCPR Sensor contains electronic compo-
nents. 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.
Warranty
Refer to the Laerdal Global Warranty for terms
and conditions. For more information visit www.
laerdal.com
Symbol Glossary
CE mark
UKCA mark
Australian Radiocommunications
and EMC Compliance Mark
KC (Korea Certification)
certification mark
Japanese MIC Certification
WEEE mark
Manufacturer
Date of Manufacture
Reference Order Number
LOT Number
Specications
Operating
temperature
5 °C to 35 °C (41 °F to 95 °F)
Degradation in product
performance may be
experienced when used at low
temperatures (< 15 °C / 59 °F)
Storage
temperature
-10 °C to 50 °C
(14 °F to 122 °F)
Humidity 5 % - 95 % relative humidity
Weight 1.8 kg (± 0.2 kg)
Dimensions 65 x 26 x 14 cm
(25 x 10 x 5 inches)
PB
20-15510 Rev D
www.laerdal.com
© 2022 Laerdal Medical AS. All rights reserved.
Manufactured in China for:
Laerdal Medical AS
P.O. Box 377
Tanke Svilandsgate 30, 4002 Stavanger, Norway
T: (+47) 51 51 17 00
Printed in China
Little Baby
QCPR
www.laerdal.com
2
QCPR
QCPR
3
QCPR
QCPR
QCPR Instructor
QCPR Learner
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