Gima LAERDAL LITTLE BABY QCPR User guide

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Little Baby QCPR
Important Product Information
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重要产品信息
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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 injur y 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.
English
Little Baby QCPR
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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Little Baby QCPR
Federal Communications Commission (FCC) and Industry Canada (IC) State­ments
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 licence­exempt 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
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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 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.
Warranty
Refer to the Laerdal Global Warranty for terms and conditions. For more information visit www.
laerdal.com
Little Baby QCPR
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
Specications
Operating temperature
Storage temperature
Humidity 5 % - 95 % relative humidity
Weight 1.8 kg (± 0.2 kg)
Dimensions 65 x 26 x 14 cm
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)
-10 °C to 50 °C (14 °F to 122 °F)
(25 x 10 x 5 inches)
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© 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
www.laerdal.com
20-15510 Rev D
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Little Baby
QCPR
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QCPR
QCPR
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QCPR
QCPR
QCPR Instructor QCPR Learner
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www.laerdal.com/support
© 2019 Laerdal Medical AS. All rights reserved.
Laerdal Medical AS P.O. Box 377, Tanke Svilandsgate 30, 4002 Stavanger, Norway T: (+47) 51 51 17 00
Printed in China
www.laerdal.com
20-15511 Rev A
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