QHQ-197AEDTAED Trainer

www.laerdal.com AED Important Product Information 重要产品信息 EN FR DE ES BR NL NO SE DA IT FI JA ZH KO PL English AED Important Information 23 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 AED Trainer clean and in a hygienic condition. Wipe the device with a clean cloth dampened with clean water, or Laerdal manikin wipes, then leave to dry. 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 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. English AED Important Information 3 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 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. 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. Canada This Class B digital apparatus complies with Canadian ICES-003. English AED Important Information 45 EU 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 UKCA (U.K. Conformity Assessed): This product complies with the requirements of U.K. legislation of Radio Equipment Regulations (S.I. 2017/1206). 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 di…

Text truncated - open the document above for the full version.

Form: RFT-AMER-TCB-OP-19o Revision: 1 Page 1 of 1 Date: 1/25/2023 Attention: Application Examiner Re: Certification designating a U.S. agent for service of process pursuant to section 2.911(d)(7) of the FCC rules To whom it may concern, This letter is to confirm both Laerdal Medical Corporation (“Agent”) and Laerdal Medical AS (“Applicant”) acknowledge consent to obligations of each party pursuant to 47 CFR part §2.911(d)(7) of the FCC rules in regard to the agent for service of process. I Mari Kaada HEREBY CERTIFY THAT I am authorized to make the representations above on behalf of the Applicant. I further acknowledge the requirement to maintain an agent extends for no less than one year after the termination of all marketing and importation or the conclusion of and commission-related proceeding involving the equipment and agree to immediately notify the FCC and Intertek if there is any change in the status identified above. Applicant Company Name : Laerdal Medical AS Contact Name : Mari Kaada Address : Tanke Svilands gate 30, P.O. Box 377, 4002 Stavanger, Norway Telephone No : +47 51 51 16 30 Email : [email protected] FCC ID : QHQ-197AEDT Applicant FRN : 0007349657 Signature: ____________________________________ Date: ____________________________________ I Don Garrison HEREBY CERTIFY THAT I am authorized to make the representations above on behalf of the Agent. I consent to the obligation to accept service of process on behalf of the applicant in regard to the FCC ID designated above. Agent Company Name : Laerdal Medical Corporation Contact Name : Don Garrison Address : 167 Myers Corners Road, Wappingers Falls, New York, NY, 12590, USA Telephone No : +18452966466 Email : [email protected] Agent FRN : 0033964867 Signature: ____________________________________ Date: ____________________________________ DocuSign Envelope ID: 6F482905-8A12-499F-BB81-88D7B4E1E6C3 03.07.2023 03.07.2023 Certificate Of Completion Envelope Id: 6F4829058A12499FBB8188D7B4E1E6C3Status: Completed Subject: Please DocuSign This Document Source Envelope: Document Pages: 1Signatures: 2Envelope Originator: Certificate Pages: 2Initials: 0Michal Zamojski AutoNav: Enabled EnvelopeId Stamping: Enabled Time Zone: (UTC+01:00) Amsterdam, Berlin, Bern, Rome, Stockholm, Vienna Tanke Svilandsgate 30 Stavanger, Stavanger 4002 [email protected] IP Address: 185.81.101.11 Record Tracking Status: Original 2023-07-03 | 14:26 Holder: Michal Zamojski [email protected] Location: DocuSign Signer EventsSignatureTimestamp Don Garrison [email protected] Laerdal Medical AS Security Level: Email, Account Authentication (None) Signature Adoption: Drawn on Device Using IP Address: 24.186.244.155 Sent: 2023-07-03 | 14:27 Viewed: 2023-07-03 | 15:24 Signed: 2023-07-03 | 15:25 Electronic Record and Signature Disclosure: Not Offered via DocuSign Mari Kaada [email protected] Corporate Director Q&R Laerdal Medical AS Security Level: Email, Account Authentication (None) Signature Adoption: Pre-selected Style Using IP Address: 88.93.180.128 Sent: 2023-07-03 | 14:27 Viewed: 2023-07-03 | 15:42 Signed: 2023-07-03 | 15:43 Electronic Record and Signature Disclosure: Not Offered via DocuSign In Person Signer EventsSignatureTimestamp Editor Delivery EventsStatusTimestamp Agent Delivery EventsStatusTimestamp Intermediary Delivery EventsStatusTimestamp Certified Delivery EventsStatusTimestamp Carbon Copy EventsStatusTimestamp Witness EventsSignatureTimestamp Notary EventsSignatureTimestamp Envelope Summary EventsStatusTimestamps Envelope SentHashed/Encrypted2023-07-03 | 14:27 Certified DeliveredSecurity Checked2023-07-03 | 15:42 Signing CompleteSecurity Checked2023-07-03 | 15:43 Envelope Summary EventsStatusTimestamps CompletedSecurity Checked2023-07-03 | 15:43 Payment EventsStatusTimestamps

Front Back Top Bottom Left Right

Legend Reference geometries Laser engraved graphics Notes Regulatory info AED Trainer Laser engraving graphics - Back Drawing is in 1:1 scale Units in mm Tolerances ± 0.5 mm This data changes per single unit: 5 5 4 4 AI Full title Format Data Title Use 01 Global Trade Item Number n2+n14 GTIN If quantity is sellable unit is 1 11 Manufacturing Date N2+n6 Manufacturing Date If product is not LOT or SN controlled 21 Serial Number n2+an..20 SERIAL If product is serial number controlled GS1 Data Matrix (in accordance with ISO 15415:2011 GRADE C or better if specied on work order) and human readable format of the GS1 code, including GTIN and other Serial Number <SN Regulatory Information - to be added when applicable. Symbols (min Ø5 mm): • WEEE Bin • CE mark • UKCA mark • MIC mark + ID: 012-23XXXX • KC mark • RCM mark ID’s: • CMIIT ID: 2023DJXXXXX • KC ID: R-R-Lm1-197AEDT • FCC ID: QHQ-197AEDT • IC: 20263-197AEDT FCC ID: xxxxxxxxxxx IC ID: xxxxxxxxxxxxx BARCODE SYMBOLIC Datamatrix w/AL’s, Height = GTIN+SERIAL/ PROD.DATE (01) 0704543XXXXXXK (11/21) 123456789012345678 HVIN: 20-18692 Cat.no.: 197-01050 xxxxxxxxxxxx CMIIT ID: xxxxxxxxxxx KC ID: xxxxxxxxxxxxxxx Laerdal Medical AS, P.O. Box 377, Tanke Svilandsgate 30 4002 Stavanger, Norway Made in China xxxxxxxxxx

Trade Register Munich HRB 85742 VAT ID No. DE129484267 Information pursuant to Section 2(1) DL-InfoV (Germany) at www.tuev-sued.com/im print Managing Directors: Walter Reithmaier (CEO) Patrick van Welij Phone: +49 (0) 9421 55 22-0 Fax: +49 (0) 9421 55 22-199 www.tuev-sued.de TÜV SÜD Product Service GmbH Äußere Frühlingstraße 45 94315 Straubing Germany TÜV SÜD Product Service RESPONSIBLE FOR NAME DATE SIGNATURE Project Management Alex Fink 2023-02-27 SIGN-ID 763206 Authorised Signatory Matthias Stumpe 2023-02-27 SIGN-ID 763892 Signatures in this approval box have checked this document in line with the requirements of TÜV SÜD Product Service document control rules. ENGINEERING STATEMENT The measurements shown in this report were made in accordance with the procedures described on test pages. All reported testing was carried out on a sample equipment to demonstrate limited compliance with FCC 47 CFR Part 1.1310, Part 2.1093 and RSS 102 Issue 5 (March 2015) + Amendment 1 (February 2021). The sample tested was found to comply with the requirements defined in the applied rules. RESPONSIBLE FOR NAME DATE Testing Alex Fink 2023-02-27 SIGN-ID 763206 Laboratory Accreditation DAkkS Reg. No. D-PL-11321-11-03 DAkkS Reg. No. D-PL-11321-11-04 Laboratory recognition Registration No. BNetzA-CAB-16/21-15 ISED Canada test site registration 3050A-2 EXECUTIVE SUMMARY A sample of this product was tested and found to be compliant with FCC 47 CFR Part 1.1310, Part 2.1093 and RSS 102 Issue 5 (March 2015) + Amendment 1 (February 2021) Report on the FCC and IC Testing of the Laerdal Medical AS Model: AED Trainer In accordance with FCC 47 CFR Part 1.1310, Part 2.1093 and RSS-102 Prepared for: Laerdal Medical AS Tanke Svilands gate 30 4007 Stavanger Norway FCC ID: QHQ-197AEDT IC: 20263-197AEDT COMMERCIAL-IN-CONFIDENCE Date: 2023-02-27 Document Number: TR-713293041-03 | Revision 0 DISCLAIMER AND COPYRIGHT This non-binding report has been prepared by TÜV SÜD Product Service with all reasonable skill and care. The document is confidential to the potential Client and TÜV SÜD Product Service. No part of this document may be reproduced without the prior written approval of TÜV SÜD Product Service. © 2023 TÜV SÜD Product Service. ACCREDITATION Our BNetzA Accreditation does not cover opinions and interpretations and any expressed are outside the scope of our BNetzA Accreditation. Document Number: TR- TR-713293041-03 | Revision 0 COMMERCIAL-IN-CONFIDENCE COMMERCIAL-IN-CONFIDENCE Page 1 of 9 Contents 1 Report Summary .........................................................................................................................2 1.1 Report Modification Record ...........................................................................................................2 1.2 Introduction ....................................................................................................................................2 1.3 Brief Summary of Results .............................................................................................................3 1.4 EUT Modification Record ..............................................................................................................4 1.5 Test Location .................................................................................................................................4 2 Test Details ..................................................................................................................................5 3 Measurement Uncertainty ..........................................................................................................6 Document Number: TR- TR-713293041-03 | Revision 0 COMMERCIAL-IN-CONFIDENCE COMMERCIAL-IN-CONFIDENCE Page 2 of 9 1 Report Summary 1.1 Report Modification Record Alterations and additions to this report will be issued to the holders of each copy in the form of a complete document. Issue Description of Change Date of Issue 0 First Issue 2023-02-27 Table 1 1.2 Introduction Applicant Laerdal Medical AS Manufacturer Laerdal Medical AS Model Number(s) AED Trainer Serial Number(s) 3140497-0038 Hardware Version(s) --- Software Version(s) --- Number of Samples Tested 1 Test Specification/Issue/Date FCC 47 CFR Part 1.1310 and Part 2.1093 RSS 102 Issue 5 (March 2015) + Amendment 1 (February 2021) Test Plan/Issue/Date --- Order Number Date N/A 2023-01-31 Date of Receipt of EUT 2023-02-02 Start of Test 2023-02-06 Finish of Test 2023-02-06 Name of Engineer(s) Alex Fink Related Document(s) 447498 D04 Interim General RF Exposure Guidance v01 ANSI C63.10 (2013) Document Number: TR- TR-713293041-03 | Revision 0 COMMERCIAL-IN-CONFIDENCE COMMERCIAL-IN-CONFIDENCE Page 3 of 9 1.3 Brief Summary of Results A brief summary of the tests carried out in accordance with FCC 47 CFR Part 1.1310, Part 2.1093 and RSS-102 is shown below. Section Specification Clause Test Description Result Comments/Base Standard Configuration and Mode: Continuously Transmitting with modulation 2.1 1.1310 2.5.1, 2.5.2, 3 RF Exposure Evaluation Pass KDB 447498 D01 v07 Table 2 Document Number: TR-713293041-03 | Revision 0 COMMERCIAL-IN-CONFIDENCE COMMERCIAL-IN-CONFIDENCE Page 4 of 9 1.4 EUT Modification Record The table below details modifications made to the EUT during the test programme. The modifications incorporated during each test are recorded on the appropriate test pages. Modification State Description of Modification still fitted to EUT Modification Fitted By Date Modification Fitted 0 As supplied by the customer (S/N: 3140497- 0038) Not Applicable Not Applicable Table 3 1.5 Test Location TÜV SÜD Product Service conducted the following tests at our Straubing Test Laboratory. Test Name Name of Engineer(s) Configuration and Mode: Continuously Transmitting with modulation RF Exposure Evaluation Alex Fink Table 4 Office Address: Äußere Frühlingstraße 45 94315 Straubing Germany Document Number: TR-713293041-03 | Revision 0 COMMERCIAL-IN-CONFIDENCE COMMERCIAL-IN…

Text truncated - open the document above for the full version.

Trade Register Munich HRB 85742 VAT ID No. DE129484267 Information pursuant to Section 2(1) DL-InfoV (Germany) at www.tuev-sued.com/imprint Managing Directors: Walter Reithmaier (CEO) Patrick van Welij Phone: +49 (0) 9421 55 22-0 Fax: +49 (0) 9421 55 22-199 www.tuev-sued.de TÜV SÜD Product Service GmbH Äußere Frühlingstraße 45 94315 Straubing Germany TÜV SÜD Product Service RESPONSIBLE FOR NAME DATE SIGNATURE Project Management Alex Fink 2023-02-27 SIGN-ID 763135 Authorised Signatory Matthias Stumpe 2023-02-28 SIGN-ID 763891 Signatures in this approval box have checked this document in line with the requirements of TÜV SÜD Product Service document control rules. ENGINEERING STATEMENT The measurements shown in this report were made in accordance with the procedures described on test pages. All reported testing was carried out on a sample equipment to demonstrate limited compliance with FCC 47 CFR Part 15C and ISED Canada RSS-247 and ISED Canada RSS-GEN. The sample tested was found to comply with the requirements defined in the applied rules. RESPONSIBLE FOR NAME DATE SIGNATURE Testing Alex Fink 2023-02-27 SIGN-ID 763135 Laboratory Accreditation DAkkS Reg. No. D-PL-11321-11-03 DAkkS Reg. No. D-PL-11321-11-04 Laboratory recognition Registration No. BNetzA-CAB-16/21-15 ISED Canada test site registration 3050A-2 EXECUTIVE SUMMARY A sample of this product was tested and found to be compliant with FCC 47 CFR Part 15C, ISED Canada RSS-247, Issue 2 (2017- 02) and ISED Canada RSS-GEN:2016, Issue 5 (2019-03). DISCLAIMER AND COPYRIGHT This non-binding report has been prepared by TÜV SÜD Product Service with all reasonable skill and care. The document is confidential to the potential Client and TÜV SÜD Product Service. No part of this document may be reproduced without the prior written approval of TÜV SÜD Product Service. © 2023 TÜV SÜD Product Service. ACCREDITATION Our BNetzA Accreditation does not cover opinions and interpretations and any expressed are outside the scope of our BNetzA Accreditation. Report on the FCC and IC Testing of the Laerdal Medical AS Model: AED Trainer In accordance with FCC 47 CFR Part 15C, ISED Canada RSS-247 and ISED Canada RSS-GEN Prepared for: Laerdal Medical AS Tanke Svilands gate 30 4007 Stavanger Norway FCC ID: QHQ-197AEDT IC: 20263-197AEDT COMMERCIAL-IN-CONFIDENCE Date: 2023-02-27 Document Number: TR-713293041-02 | Revision: 0 Document Number: TR-713293041-02 | Revision: 0 COMMERCIAL-IN-CONFIDENCE COMMERCIAL-IN-CONFIDENCE Page 1 of 48 Contents 1 Report Summary .........................................................................................................................2 1.1 Report Modification Record ...........................................................................................................2 1.2 Introduction ....................................................................................................................................2 1.3 Brief Summary of Results .............................................................................................................3 1.4 Basic information of EUT ..............................................................................................................4 1.5 EUT Modification Record ..............................................................................................................5 1.6 Test Location .................................................................................................................................5 2 Test Setup ....................................................................................................................................6 2.1 Radiated Emission in Fully or Semi Anechoic Room ....................................................................6 2.2 Radiated Emission at Alternative Test Site ...................................................................................8 3 Test Details ............................................................................................................................... 10 3.1 Spurious Emissions .................................................................................................................... 10 3.2 Restricted Band Edges............................................................................................................... 22 3.3 Authorised Band Edges ............................................................................................................. 25 3.4 Emission Bandwidth ................................................................................................................... 28 3.5 Power Spectral Density .............................................................................................................. 36 3.6 Maximum Conducted Output Power .......................................................................................... 38 3.7 Transmitter frequency stability ................................................................................................... 40 4 Photographs ............................................................................................................................. 44 4.1 Test Setup Photos ...................................................................................................................... 44 5 Measurement Uncertainty ....................................................................................................... 45 Annex: Test Setup Photos 4 pages Document Number: TR-713293041-02 | Revision: 0 COMMERCIAL-IN-CONFIDENCE COMMERCIAL-IN-CONFIDENCE Page 2 of 48 1 Report Summary 1.1 Report Modification Record Alterations and additions to this report will be issued to the holders of each copy in the form of a complete document. Revision Description of Change Date of Issue 0 First revision 2023-02-27 Table 1 1.2 Introduction Applicant Laerdal Medical AS Manufacturer Laerdal Medical AS Model Number(s) AED Trainer Serial Number(s) 3140497-0038 (conducted sample)…

Text truncated - open the document above for the full version.

Trade Register Munich HRB 85742 VAT ID No. DE129484267 Information pursuant to Section 2(1) DL-InfoV (Germany) at www.tuvsud.com/imprint Managing Directors: Walter Reitmaier (Sprecher / CEO) Patrick van Welij Phone: +49 (0) 9421 55 22-0 Fax: +49 (0) 9421 55 22-199 www.tuvsud.com TÜV SÜD Product Service GmbH Äußere Frühlingstraße 45 94315 Straubing Germany TÜV SÜD Product Service Report on Radio Testing of the Laerdal Medical AS Model: AED Trainer 2D Antenna Diagram Prepared for: Laerdal Medical AS Tanke Svilandsgate 4002 Stavanger; Norway COMMERCIAL-IN-CONFIDENCE Date: 2023-02-13 Document Number: TR-713293096-00 | Revision 0 RESPONSIBLE FOR NAME DATE SIGNATURE Project Management Martin Steindl 2023-02-13 SIGN-ID 758359 Authorised Signatory Alex Fink 2023-02-13 SIGN-ID 758419 Signatures in this approval box have checked this document in line with the requirements of TÜV SÜD Product Service document control rules. DISCLAIMER AND COPYRIGHT This non-binding report has been prepared by TÜV SÜD Product Service with all reasonable skill and care. The document is confiden- tial to the potential Client and TÜV SÜD Product Service. No part of this document may be reproduced without the prior written ap- proval of TÜV SÜD Product Service. © 2023 TÜV SÜD Product Service. Document Number: TR-713293096-00 | Revision 0 COMMERCIAL-IN-CONFIDENCE COMMERCIAL-IN-CONFIDENCE Page 1 of 17 Content 1 Report Summary.............................................................................................................................. 2 1.1 Modification Report .................................................................................................................. 2 1.2 Introduction .............................................................................................................................. 2 1.3 Brief Summary of Results ........................................................................................................ 2 1.4 Product Information ................................................................................................................. 3 1.5 Test Configuration ................................................................................................................... 3 1.6 Modes of Operation ................................................................................................................. 3 1.7 EUT Modifications Record ....................................................................................................... 4 1.8 Test Location ........................................................................................................................... 4 2 Test Details ...................................................................................................................................... 5 2.1 Antenna diagram ..................................................................................................................... 5 3 Measurement Uncertainty ............................................................................................................. 16 Annex A Detailed Test Data ..................................................................................................... 18 pages Document Number: TR-713293096-00 | Revision 0 COMMERCIAL-IN-CONFIDENCE COMMERCIAL-IN-CONFIDENCE Page 2 of 17 1 Report Summary 1.1 Modification Report Alternations and additions of this report will be issued to the holders of each copy in the form of a com- plete document. Revision Description of changes Date of Issue 0 First Issue 2023-02-13 Table 1: Report of Modifications 1.2 Introduction Applicant Laerdal Medical AS Tanke Svilands Gate 30 4002 Stavanger; Norway Manufacturer Laerdal Medical; Suzhou Model Number(s) AED Trainer Serial Number(s) N/A Hardware Version(s) N/A Software Version(s) N/A Number of Samples Tested 1 Test Specification(s) / Issue / Date ETSI EN 300 328 V2.2.2 (2019-07) Test Plan/Issue/Date N/A Order Number Date PG002359 2023-02-01 Date of Receipt of EUT 2023-02-02 Start of Test 2023-02-10 Finish of Test 2023-02-10 Name of Engineer(s) M. Steindl Related Document(s) --- 1.3 Brief Summary of Results A brief summary of the tests carried out is shown below. Section Test Description Result 2.1 Antenna Diagram Result noted Table 2: Results Document Number: TR-713293096-00 | Revision 0 COMMERCIAL-IN-CONFIDENCE COMMERCIAL-IN-CONFIDENCE Page 3 of 17 1.4 Product Information 1.4.1 General Technical Description AED trainer is used in combination with simulated AED pads. The AED pads can be used a limited number of times and are available for purchase seperately (consumable). There are several alternative simulated AED pads, ranging from dummy pads with no transfere signals or data to advance pads where there is a transfer of signals or data. Frequency Band: 2400.0 MHz – 2483.5 MHz Supply Voltage: 6 V Supply Frequency: 0 Hz (DC) Highest clock frequency (non-radio part): 64 MHz 1.4.2 EUT Ports / Cables identification Port Max Cable Length speci- fied Usage Screened DC supply 2 m DC supply No RS-232 1 m Signal/Control port Yes Table 3 1.5 Test Configuration The EUT was provided as printed board. Radiated emissions were tested with the EUT in three orthogonal positions. 1.6 Modes of Operation The EUT was configured to transmit on lowest and highest frequency channel. Document Number: TR-713293096-00 | Revision 0 COMMERCIAL-IN-CONFIDENCE COMMERCIAL-IN-CONFIDENCE Page 4 of 17 1.7 EUT Modifications Record The table below details modifications made to the EUT during the test programme. The modifications incorporated during each test are recorded on the appropriate test pages. Modification State Description of Modification still fitted to EUT Modification Fitted By Date Modification Fitted 0 As supplied by the customer Not Applicable Not Applicable Table 4 1.8 Test Location TÜV SÜD Product Service conducted the following tests at our Straubing test laboratory: Test Name Name of Engineer(s) Antenna diagram Martin Stein…

Text truncated - open the document above for the full version.

Document Number: TR-713293096-00 | Annex A | Revision 0 COMMERCIAL-IN-CONFIDENCE COMMERCIAL-IN-CONFIDENCE Page 1 of 18 Annex A DetailedTest Data A.1 Antenna diagram A.1.1 Test Results A.1.1.1 Rotating x-axis A.1.1.1.1 Horizontal polarization Azimuth Frequency 2402.000 MHz Frequency 2480.000 MHz deg dBi dBi 0.0 -16.69 -13.72 2.0 -18.19 -15.75 4.0 -11.50 -16.98 6.0 -11.50 -15.01 8.0 -8.35 -15.01 10.0 -7.18 -13.47 12.0 -7.18 -11.15 14.0 -5.13 -11.15 16.0 -4.48 -8.50 18.0 -4.48 -8.50 20.0 -3.69 -7.15 22.0 -3.69 -4.96 24.0 -3.21 -4.96 26.0 -2.89 -3.70 28.0 -2.88 -3.70 30.0 -2.04 -2.80 32.0 -2.04 -2.80 34.0 -1.19 -2.36 36.0 -1.19 -1.80 38.0 -0.76 -1.80 40.0 -0.80 -1.65 42.0 -0.80 -1.56 44.0 -1.36 -1.48 46.0 -1.36 -1.27 48.0 -2.22 -1.27 50.0 -2.60 -1.14 52.0 -2.60 -1.14 54.0 -3.41 -1.19 56.0 -3.41 -1.41 58.0 -4.41 -1.41 60.0 -4.82 -1.50 62.0 -4.82 -1.72 64.0 -5.4…

Text truncated - open the document above for the full version.