Laerdal AED Trainer Instructions

Laerdal AED Trainer

Product Information

The product is an AED (Automated External Defibrillator) Trainer. It is designed to simulate the operation of a real AED and provide training for users on how to respond to cardiac emergencies.

Important Product Information
It is important to read and understand the following instructions:

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

Warnings and Cautions

Warnings:

• A Warning indicates a condition, hazard, or unsafe practice that can result in serious personal injury or death.

Cautions:

• A Caution indicates 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

To ensure proper functionality and hygiene:

• Keep the AED Trainer clean and in a hygienic condition.
• Wipe the device with a clean cloth dampened with clean water or Laerdal manikin wipes.
• Allow the device to dry after cleaning.

Cautions

• Do not submerge in any liquid
• Do not operate in rain or near water
• Do not operate in areas with a high concentration of dust

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 certain conditions:

• The device may not cause harmful interference.
• The device must accept any interference received, including interference that may cause undesired operation.
• Changes or modifications not 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.
• 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 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.

Canada
This Class B digital apparatus complies with Canadian ICES-003.

European Union (EU) Compliance

The product is in compliance with the following directives:

• Council Directive 2014/53/EU on Radio Equipment (RED)
• Council Directive 2011/65/EU on restriction of the use of certain hazardous substances (RoHS)

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).

UK Compliance
The product complies with the requirements of U.K. legislation:

• U.K. Conformity Assessed (UKCA): U.K. legislation of Radio Equipment Regulations (S.I. 2017/1206)
• Restriction of the Use of Certain Hazardous Substances in Electrical and Electronic Equipment Regulations (RoHS) Regulations (S.I. 2012/3032)

Waste Handling
Dispose of the product in accordance with your country’s recommendations:

• Follow the European directive 2012/19/EC on Waste Electrical and Electronic Equipment (WEEE).
• Do not treat the appliance as household waste.
• Hand it over to the applicable collection point for recycling of electrical and electronic equipment.
• Dispose of it in accordance with local environmental regulations for waste disposal.

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.

Battery

The following battery types are recommended:

• Non-rechargeable alkaline batteries, LR6 1.5 V AA
• Rechargeable NiMH batteries, HR6 1.2 V AA

Warnings

• Batteries must be replaced with correct type
• Do not use batteries with a nominal cell voltage higher than 1.5 V
• Remove batteries if product is not to be used for an extended period

Notes

• If the device is used with rechargeable batteries, the “Low battery warning” deviates from normal behavior
• Internal charging is not supported.

Symbol Glossary

Specifications

Size and Weight

Dimensions| 20 x 14 x 4.1 cm (7.9 x 5.5 x 1.6 Inches)
Weight| 0.5 kg (± 0.05 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 (< 15 °C / 59 °F)
Storage temperatures| -10 °C to 50 °C
(14 °F to 122 °F)
Relative humidity| 5 % – 95 % relative humidity

Warranty
Refer to the Laerdal Global Warranty for terms and conditions. For more information visit www.laerdal.com
© 2023 Laerdal Medical AS. All rights reserved.
Manufactured by Laerdal Medical AS,
P.O. Box 377
Tanke Svilandsgate
30, 4002 Stavanger,
Norway
T: (+47) 51 51 17 00

References

• Welcome to Laerdal Medical – Helping Save Lives | Laerdal Medical
• Welcome to Laerdal Medical – Helping Save Lives | Laerdal Medical
• Welcome to Laerdal Medical – Helping Save Lives | Laerdal Medical
• Bem-vindos à Laerdal Medical – Helping Save Lives | Laerdal Medical

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