Laerdal Little Anne Plus QCPR Dark Skin Training Manikins User Manual

: June 9, 2024
: Laerdal

Table of Contents

How to use
Important Information
References
Read User Manual Online (PDF format)
Download This Manual (PDF format)

Laerdal Little Anne Plus QCPR Dark Skin Training Manikins

Laerdal Little Anne Plus QCPR Dark Skin Training
Manikins

How to use

Important Information

Read these instructions thoroughly. Observe all warnings, cautions and instructions in the User Guide and in this Important Product Information booklet. Retain this booklet for future reference.

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, Maintanance and Cleaning

Keep the manikin clean and in a hygienic condition.
Replace the airway filter after every class, especially if mouth to mouth resuscitation is practiced.
Change the airway assembly if there are visible signs of wear or damage to lung or metal patch.
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.
Do not remove the spring plate rope.

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:

This device may not cause harmful interference, and
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 occurin 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.

FCC ID: QHQ -LA
IC: 20263-LA
Japan MIC certification 012-220014
Korea R-CMM-Lm1-LA
China Basic Torso: CMIIT ID: xxxxxxxxxx
This product is in compliance with the essential requirements of Council Directive 2014/53/EU on Radio Equipment (RED), The product is in compliance with Council Directive 2011/65/EU on restriction of the use of certain hazardous substances (RoHS).

KCA (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

Dispose of in accordance with your country’s recommendations.
This appliance is marked according to the European directive 2012/19/EC 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 Laerdal representative.

Symbol Glossary

Symbol Definition

Warranty

Refer to the Laerdal Global Warranty for terms and conditions. For more information visit www.laerdal.com

Specifications

Size and Weight

Dimensions| 64 cm x 37 cm x 21,5 cm (25.2” x 14.5” x 8.5”)
Weight| 2 kg (± 0.2 kg)
Environment
Operating temperatures| 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 temperatures| -10 °C to 50 °C (14 °F to 122 °F)
Relative humidity| 5 % – 95 % relative humidity

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

For more informationand apps go to: laerdal.com/littleanne

www.laerdal.com

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