QHQ-185-20050Defibrillator Training System with Bluetooth Low Energy communication

ShockLink Important Product Information EN www.laerdal.com 23 English ShockLink Important Information 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 manikin. Notes Important information about the product or its operation. Cautions • Maximum energy in one shock: 360 J (Only give a cumulative total of 1,000 J per minute.) ShockLink will disconnect the defibrillator for one minute if a cumulative total of more than 4000 J has been given over the last 3 minutes • Do not use ShockLink if the cable or the housing has visible damage or openings. • Do not use ShockLink in wet conditions. Waste Handling The ShockLink unit contains electronic components. Dispose of it at the applicable recycling facility in accordance with local regulations. 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. 3 English ShockLink Important Information FCC Federal Communications Commission Statement and Industry Canada Statements This device complies with part 15 of the FCC rules and RSS-210 of the Industry Canada 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. Ce dispositif est conforme à la norme CNR-210 d’Industrie Canada applicable aux appareils radio exempts de licence. Son fonctionnement est sujet aux deux conditions suivantes: 1. Le dispositif ne doit pas produire de brouillage préjudiciable, et 2. ce dispositif doit accepter tout brouillage reçu, y compris un brouillage susceptible de provoquer un fonctionnement indésirable. 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. FCC ID: QHQ-185-20050 IC ID: 20263-18520050 The term ”IC” before the equipment certification number only signifies that the Industry Canada technical specifications were met. Caution Changes or modifications not expressly approved by Laerdal Medical could void the user’s authority to operate the equipment. 45 English ShockLink Important Information Symbol Glossary ShockLink is CE marked in accordance with Council Directive 1999/5/EC relating to Radio and Telecommunications Terminal Equipment (R&TTE), and Council Directive 2011/65/EU on Restriction on the use of certain hazardous substance (RoHS). Australian Radiocommunications and EMC Compliance Mark Dispose of in accordance with your country’s recommendations FCC Statement and IC statements Reference order number Production lot number Specifications Dimensions 85 x 53 x 14 mm (3.3 x 2 x 0.5”) Weight120 g (0.26 lbs) (including battery) Cable lengthApproximately 0.9 m (3ft) Defibrillator impedance115 Ohms Operation temperature0 °C to +35 °C (32 °F to 95 °F) Storage temperature-15 °C to +50 °C (5 °F to 122 °F) Humidity< 95% relative humidity non condensing CommunicationBluetooth Smart BatteryAAA size Alkaline battery 1.5 V Battery lifeON: 25 - 35 hours OFF: 3 years (shelf life with battery mounted) Battery Low warning:@ 1.1 V, typically 4 hours left Unit turns off:@ 0.95 V nominal Shock detection:5 – 360 J, +/- 15% Warranty Refer to the Laerdal Global Warranty for terms and conditions. For more information visit www.laerdal.com 5 ShockLink® Patent Pending Laerdal Medical, the Laerdal logo and ShockLink are trademarks owned by Laerdal Medical AS. © 2015 Laerdal Medical AS. All rights reserved. Manufacturer : Laerdal Medical AS P.O. Box 377 Tanke Svilandsgt. 30, 4002 Stavanger, Norway T: (+47) 51 51 17 00 Printed in China. 20-09356 Rev A www.laerdal.com

Shocklink Label Label size: 14 x 50 mmPrinting: Laser engraving.

ShockLink Operation Description. Page 1 of 3 ShockLink Operation Description. ShockLink enables rescuers to train with defibrillators in the way clinical procedures are carried out. ShockLink connects to a defibrillator in one end. The other end of ShockLink connects to self adhesive training pads, intended to be placed on training manikins. Depending on the state of the training electrodes, the defibrillator will see an open circuit or a connected patient. With a connected patient ShockLink will generate ECG to the defibrillator. ShockLink accepts high voltage shocks from the defibrillator which are absorbed in the attachment cable. No defibrillator voltages or energy appear on the training pads side. The ECG rhythm and other functions can be controlled from an infrared Remote Control, a Smart Phone using Bluetooth Smart (BLE) communication or through wired communication over the training pads. System Description Defibrillator Laerdal Link ECG library ECG selection LED indication ? Manikin VDD 1 VDD 12 V S S 1 3 VDD_PA 30 ANT1 31 ANT2 32 VSS 33 VSS 34 AVDD 35 AVDD 36 X C1 37 X C2 38 nRF51822 DCC 2 P0.30 3 P0.00 4 P0.01 5 P0.02 6 P0.03 7 P0.04 8 P0.05 9 P0.06 10 P0.07 11 P 0.08 1 4 P 0.09 1 5 P 0.10 1 6 P 0.11 1 7 D E C1 39 P 0.21 40 P 0.22 41 P 0.23 42 P 0.24 43 P 0.25 44 P 0.27 46 P 0.26 45 P 0.29 48 P 0.28 47 P0.17 25 P0.18 26 P0.19 27 P0.20 28 DEC2 29 P 0.12 1 8 P 0.13 1 9 P 0.14 2 0 P 0.15 2 1 S W D IO /n RE S E T 2 3 S W D C L K 2 4 P 0.16 2 2 U1 nRF51822-QFAA IR Rec Laerdal Link R X / T X Electrode detect Defibrillator Interface -ECG -Electrode connection switch -Energy measurement -Pacing current measurement -ON Detection Boost 3V3 White LED Safety capacitor Isolation Resistance cable Boost 12V Blue LED Pads Bluetooth Low Energy (BLE) ShockLink Operation Description. Page 2 of 3 Power supplies: Powered by a 1.5 V AAA alakaline battery. Typical power consumption 30 mA @ 1.5 V. Internal power supplies: 3. 3 V and 12V. MicroController: Nordic Semiconductor nRF51822 Multiprotocol Bluetooth® 4.0 low energy/2.4 GHz RF System on Chip. Defibrillator interface: Circuitry for detecting defibrillator impedance measurement signals to be used to turn unit on. Present open circuit to a defibrillator, and present a realistic patient circuit with ECG when the training pads are connected to the manikin. Use a resistance cable as the defibrillation energy deposit (load) Detect and measure delivered defibrillation energy and pacing current. Laerdal Link: Communication towards manikin through training electrodes Safety barrier on training electrodes to prevent electrical hazard from delivered shock. Infrared: Infrared remote control receiver. Vischay TSOP75238 LEDs: White and Blue LED indicators. Radio: Bluetooth Smart (BLE) communication towards mobile phone or other controller device. Radio integrated in nRF51822 Multiprotocol Bluetooth® 4.0 low energy/2.4 GHz RF System on Chip. • Balloon: 2450BM14E0003 Johanson Technology 2.45GHz Impedance Matched Balun + Band Pass Filter: Optimized for Nordic's Chipset nRF51822 and nRF51422. ShockLink Operation Description. Page 3 of 3 • Antenna: 2450AT18A100 Johanson Technology.

Date of issue: 2015 Tested by: This report is for the exclusive use of I Intertek assumes no liability to any party, other than to the Clie distribution of this report and then only in its entirety. Any use of the Intertek name or one of observations and test results in this report are relevant only to the sample tested. This report by itself does not imply EQUIPMENT UNDER TEST Equipment: Type/Model: Manufacturer: Tested by request of: SUMMARY Referring to the emission limits, and the operating mode during the tests specified in this report, the equipment complies with the requirements accordi 47 CFR Part 15 (2014):, Subpart C: Intentional radiators. For details, see clause 2 Date of issue: 2015-0 Tested by: Daniel Nilsson This report is for the exclusive use of Intertek's Client and is provided pursuant to the agreement between Intertek and its Client. Intertek's responsibility and lia Intertek assumes no liability to any party, other than to the Clie distribution of this report and then only in its entirety. Any use of the Intertek name or one of observations and test results in this report are relevant only to the sample tested. This report by itself does not imply EQUIPMENT UNDER TEST Equipment: Type/Model: Manufacturer: Tested by request of: SUMMARY Referring to the emission limits, and the operating mode during the tests specified in this report, the equipment complies with the requirements accordi 47 CFR Part 15 (2014):, Subpart C: Intentional radiators. For details, see clause 2 07-01 Daniel Nilsson ntertek's Client and is provided pursuant to the agreement between Intertek and its Client. Intertek's responsibility and lia Intertek assumes no liability to any party, other than to the Client in accordance with the agreement, for any loss, expense or damage occasioned by the use of this report. Only the Client is distribution of this report and then only in its entirety. Any use of the Intertek name or one of observations and test results in this report are relevant only to the sample tested. This report by itself does not imply RADIO TEST REPORT No. EQUIPMENT UNDER TEST Tested by request of: Referring to the emission limits, and the operating mode during the tests specified in this report, the equipment complies with the requirements accordi 47 CFR Part 15 (2014):, Subpart C: Intentional radiators. For details, see clause 2– 4. ntertek's Client and is provided pursuant to the agreement between Intertek and its Client. Intertek's responsibility and lia nt in accordance with the agreement, for any loss, expense or damage occasioned by the use of this report. Only the Client is distribution of this report and then only in its entirety. Any use of the Intertek name or one of observations and test results in this report are relevant only to the sample tested. This report by itself does not imply RADIO TEST REPORT No.1511404STO RF Performance Defibrillator Training System with Bluetooth Low Energy communication Shocklink Laerdal Medical Laerdal Medica Referring to the emission limits, and the operating mode during the tests specified in this report, the equipment complies with the requirements accordi 47 CFR Part 15 (2014):, Subpart C: Intentional radiators. Approved by: ntertek's Client and is provided pursuant to the agreement between Intertek and its Client. Intertek's responsibility and lia nt in accordance with the agreement, for any loss, expense or damage occasioned by the use of this report. Only the Client is distribution of this report and then only in its entirety. Any use of the Intertek name or one ofits marks for the sale or advertisement of the tested material, product or service must first be approved in writing by Inter observations and test results in this report are relevant only to the sample tested. This report by itself does not imply RADIO TEST REPORT 1511404STO- RF Performance Defibrillator Training System with Bluetooth Low Energy communication Laerdal Medical Laerdal Medical Referring to the emission limits, and the operating mode during the tests specified in this report, the equipment complies with the requirements accordi 47 CFR Part 15 (2014):, Subpart C: Intentional radiators. Approved by: Matti Virkki ntertek's Client and is provided pursuant to the agreement between Intertek and its Client. Intertek's responsibility and lia nt in accordance with the agreement, for any loss, expense or damage occasioned by the use of this report. Only the Client is its marks for the sale or advertisement of the tested material, product or service must first be approved in writing by Inter observations and test results in this report are relevant only to the sample tested. This report by itself does not implythat the material, product, or service is or has ever been under an Intertek certification program RADIO TEST REPORT -001, Ed. RF Performance Defibrillator Training System with Bluetooth Low Energy communication Referring to the emission limits, and the operating mode during the tests specified in this report, the equipment complies with the requirements according to the following standards: 47 CFR Part 15 (2014):, Subpart C: Intentional radiators.Section 15.247 Matti Virkki ntertek's Client and is provided pursuant to the agreement between Intertek and its Client. Intertek's responsibility and liability are limited to nt in accordance with the agreement, for any loss, expense or damage occasioned by the use of this report. Only the Client is its marks for the sale or advertisement of the tested material, product or service must first be approved in writing by Inter that the material, product, or service is or has ever been under an Intertek certification program RADIO TEST REPORT 001, Ed.2 Defibrillator Training System with Bluetooth Low Referring to the emission limits, and the operating mode during the tests specified in this ng to the following standards: ection 15.247 Page bility are limited tothe terms and conditions of the nt in accordance with the agreement, fo…

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