Laerdal M56509FR Little Baby QCPR Instruction Manual

June 15, 2024
Laerdal

Laerdal - logo M56509FR Little Baby QCPR
Instruction Manual

M56509FR Little Baby QCPR

Laerdal M56509FR Little Baby QCPR - figLaerdal
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M56509FR Little Baby QCPR - fig 8This 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 Lardil 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 Lardil 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.\
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.
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.

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
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 electrical 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
Operating temperature| 5 °C to 35 °C (41 °F to 95 °F) Degradation in product performance may be 5experienced 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)

Laerdal - logo© 2019 Lardil Medical AS. All rights reserved.
Lateral Medical AS
P.O. Box 377,
Tanka Svilandsgate 30, 4002 Stavanger, Norway
T: (+47) 51 51 17 00
Printed in China
www.laerdal.comwww.laerdal.com/support

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