ISEIPSR434MHz International Patient Security Receiver

Service Light The red service light is located on the lower side of the Receiver, next to the service pin, and is used for troubleshooting. Red Service LED state Description OffNormal operation. Flashing every 0.5 sec. Unconfigured Receiver. Run Auto Configure using the PS System Man- ager. OnFailure. Check power supply to the device. Download Neuron firmware to the Receiver using the PS System Manager. Momentarily on Service pin pressed. Warranty Stanley Healthcare Solutions’ products are warranted against defects in materials and workmanship and shall perform in accordance with published specifications for a period of one year. Stanley Healthcare Solutions’ warranty is limited solely to the repair or replacement of the defective part or product. Stanley Healthcare Solutions reserves the right to change product specifications without notice. Limitation of Liability This Product has been designed for use to assist in the preven- tion of patient abduction and/or wandering incidents. The range, accuracy, function and performance of this Prod- uct may vary from the published specifications due to many factors, including, but not limited to, site impairments from structural effects, metal objects in the vicinity, placement of the receiver and transmitter, interference from other electrical devices, atmospheric effects, installation, and maintenance. There may be other factors, which also affect performance of this Product. XMARK Corporation (“XMARK”) does not guarantee that this Product will detect 100% of patient abductions and/or wandering incidents, nor does XMARK guarantee that this Product will not return false reports of calls for patient abduc- tions and/or wandering incidents. Monthly testing and maintenance of this Product, as described in the Product documentation, is essential to verify the system is operating correctly and to ensure that the probability of detect- ing an alarm and/or locating the transmitter are maximized. The failure to undertake regular testing and maintenance will increase the risk of system failure and failure to detect patient abductions and/or wandering incidents. The failure to under- take regular testing and maintenance will increase the risk of false reports of patient abductions and/or wandering incidents. XMARK hereby disclaims all warranties, express or implied, arising out of or in connection with any of its Products of the use or performance thereof, including but not limited to, where allowable by law, all other implied warranties or conditions of merchantability, fitness for a particular purpose, and those arising by statute or otherwise in law or from a course of dealing or usage of trade. XMARK’s liability to you or anyone claiming through or on behalf of you with respect to any claim or loss arising out of the use or misuse of XMARK’s Product, defective prod- ucts or materials, improper installation or maintenance of XMARK’s Product or products or the system in which they are incorporated, or alleged to have resulted from an act or omission of XMARK or any person, negligent or otherwise, shall be limited to the following, at XMARK’s sole option: 1) the repair or replacement of defective Product or materials supplied by XMARK during the warranty period as set out in the Product documentation; or, at the option of XMARK, 2) a refund of the purchase price of the Product supplied by XMARK. In no event shall XMARK be liable for general, specific, indirect, consequential, incidental, exemplary or punitive damages or any losses or expenses suffered by you or anyone else, whether or not XMARK, or its employees, officers, agents, resellers or installers has been informed of the risk of such loss or expense and whether or not such losses or expenses were foreseeable. Statements United States—Federal Communication Commission (FCC) This device complies with Part 15 of the FCC Rules. Opera- tion 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. NOTE: This equipment has been tested and found to comply with the limits for a Class A digital device, pursuant to Part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference when the equipment is operated in a commercial environment. This equipment generates, uses, and can radiate radio frequency energy and, if not installed and used in accordance with the instruction manual, may cause harmful interference to radio communications. Operation of this equipment in a residential area is likely to cause harmful interference in which case the user will be required to correct the interference at his own expense. Warning: Changes or modifications not expressly approved by XMARK could void the user’s authority to operate the equipment. Canada—Industry Canada The term “IC:” before the certification/registration number only signifies that Industry Canada technical specifications were met. European Union—CE Declaration XMARK hereby declares that this radio frequency receiver is in compliance with the essential requirements and other relevant provisions of the following EU directives: (1) RTTE Directive 1999/5/EC, (2) CE mark Directive 2004/108/CE, and (3) LVD 2006/95/EC. Patient Security Receiver Installation Guide Important! Have you: • Pulled network and power cable? • Resolved power supply requirements? • Selected the location for the PS Receiver? Materials Required • International Patient Security Receiver (p/n 816A1001) • Facility fl oor plan indicating Receiver position and net- work wiring path • 105 Ω network terminator (p/n 805A2401) - if this is the last device on the network segment Specifi cations Recommended Receiver Antenna Orientation For best coverage, ensure that the antennas are at least 3 ft. (91 cm) from metal objects, such as fram- ing or air ducts. Do not encase, wrap, or otherwise cover the …

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www.nemko.com Report Reference ID: 158708-1TRFWL Test specifications: Title 47-Telecommunication Chapter I - Federal Communications Commission Subchapter A - General Part 15 - Radio Frequency Devices Subpart B - Unintentional Radiators − §15.107 – Conducted limits − §15.109 – Radiated emission limits Applicant: Xmark Corporation 309 Legget Drive Ottawa, ON, Canada K2K 3A3 Apparatus: International Patient Security Receiver Model: IPSR FCC ID ISEIPSR Testing laboratory: Nemko Canada Inc. 303 River Road Ottawa, ON, Canada K1V 1H2 Telephone: (613) 737-9680 Facsimile: (613) 737-9691 Name and title Date Tested by: David Duchesne, Wireless/EMC Specialist October 27, 2010 Reviewed by: Richard Brazeau, Laboratory Manager October 27, 2010 Nemko Canada Inc., a testing laboratory, is accredited by the Standards Council of Canada. The tests included in this report are within the scope of this accreditation. Product: International Patient Security Receiver Nemko Canada Inc., 303 River Rd, Ottawa, ON, Canada, K1V 1H2 Specification: Radio disturbance Report reference ID: 158708-1TRFWL Page 2 of 19 Table of contents Section 1: Report summary.......................................................................................................................................3 1.1 Test specifications.......................................................................................................................................3 1.2 Statement of compliance.............................................................................................................................3 1.3 Exclusions....................................................................................................................................................3 1.4 Test report revision history..........................................................................................................................3 1.5 Test location................................................................................................................................................3 1.6 Limits of responsibility.................................................................................................................................3 Section 2: Summary of test results...........................................................................................................................4 2.1 FCC 47 CFR Part 15, Subpart B – Tests result summary..........................................................................4 Section 3: Equipment under test (EUT) details........................................................................................................5 3.1 Product details.............................................................................................................................................5 3.2 Sample information......................................................................................................................................5 3.3 EUT technical specifications.......................................................................................................................5 3.4 Operation of the EUT during testing............................................................................................................5 3.5 EUT setup diagram......................................................................................................................................6 Section 4: Engineering considerations....................................................................................................................7 4.1 Modifications incorporated in the EUT........................................................................................................7 4.2 Technical judgment.....................................................................................................................................7 4.3 Deviations from laboratory tests procedures...............................................................................................7 Section 5: Test conditions.........................................................................................................................................8 5.1 Normal temperature, humidity and air pressure test conditions..................................................................8 5.2 Power supply range:....................................................................................................................................8 Section 6: Measurement uncertainty........................................................................................................................9 Section 7: Test equipment.......................................................................................................................................10 7.1 Test equipment list....................................................................................................................................10 Section 8: Testing data.............................................................................................................................................11 8.1 Clause 15.109 Radiated emission limits (a)..............................................................................................11 8.2 Clause 15.107 Conducted limits (a)..........................................................................................................15 Section 9: Block diagrams of test set-ups.............................................................................................................19 Section 1: Report summary Product: International Patient Security Receiver Nemko Canada Inc., 303 River Rd, Ottawa, ON, Canada, K1V 1H2 Specification: Radio disturbance Report reference ID: 158708-1TRFWL Page 3 of 19 Section 1: Report summary 1.1 Test specifications Title 47-Telecommunication Chapter I - Federal Communications Commission Subchapter A - General Part 15 - Radio Frequency Devices Su…

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Nemko Canada Inc., 303 River Rd, Ottawa, ON, Canada, K1V 1H2 Radiated emissions set-up – Setup photos Nemko Canada Inc., 303 River Rd, Ottawa, ON, Canada, K1V 1H2 Conducted emissions set-up – Setup photos Nemko Canada Inc., 303 River Rd, Ottawa, ON, Canada, K1V 1H2 Radiated emissions set-up – Block diagram EUT 1 m 80 cm 3 m To test receiver 4 m Metal ground plane Radio absorbing material Variable search height Antenna mast Test antenna Test antenna Non-conducting Turntable Conducted emissions set-up – Block diagram EUT 80 cm Non- conducting Turntable To power supply LISN 80 cm Power cable Vertical ground plane 40 cm from EUT To test receiver