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notifier intelligent control panel slc wiring manual pdfContact Us to Register Your Interest Already a member. Product specifications are subject to change without notice. Nothing contained within this Service Manual is intended as any offer, warranty, promise, or contractual condition, and must not be taken as such. All other product names are the property of their respective owners. Reproduction in whole or in part in any form, or by any means, electrical, mechanical or otherwise, is prohibited without the written consent of the copyright holder. Philips Medical Systems 3000 Minuteman Road Andover, MA 01810 USA (978) 687-1501 Unauthorized copying of this publication may not only infringe copyright laws, but may also reduce the ability of Philips Medical Systems to provide accurate and current information to users. Compliance The Philips Medical Systems PageWriter Touch cardiograph complies with all relevant international and national standards and laws. Information on compliance will be supplied on request by a local Philips Medical Systems representative, or by the manufacturer. Intended Use of this Service Manual This Philips product is intended to be operated only in accordance with the safety procedures and operating instructions provided in this Service Manual, and in accordance with the purposes for which it was designed. Installation, use, and operation of this product is subject to the laws in effect in the jurisdiction(s) in which the product is being used. Users must only install, use, and operate this product in such a manner that does not conflict with applicable laws or regulations that have the force of law.Use of this product for purposes other than the express intended purpose provided by the manufacturer, or incorrect use and operation, may relieve the manufacturer (or agent) from all or some responsibility for resultant noncompliance, damage, or injury. United States federal law restricts this device to use by or on the order of a physician.Training requirements vary by country.http://azlawncare.com/userfiles/cram-a-lot-baler-manual.xml
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Users must ensure that they receive adequate clinical training in accordance with local laws or regulations. For further information on available training on the use of this product, please contact a Philips Medical Systems representative, or the manufacturer. This Service Manual provides information on troubleshooting, repairing, and performance verification and safety testing of the cardiograph and cart system. There is also information on the theory of operation, maintenance procedures, and ordering parts and supplies. This chapter includes general information that needs to be reviewed before servicing the PageWriter Touch cardiograph. For detailed information regarding controls, operation, and capabilities of the device, refer to the PageWriter Touch Cardiograph Instructions for Use, Edition 7 on the PageWriter Touch Cardiograph User Documentation CD (Philips part number 453564053291) or the PageWriter Touch Cardiograph Interactive Training Program on CD (Philips Part Number 989803127401). Review the PageWriter Touch Cardiograph Instructions for Use, Edition 7 before servicing this device. This Service Manual assumes knowledge of all cardiograph controls and basic features. This Service Manual provides information on troubleshooting, repairing, and performance verification and safety testing of the cardiograph and cart system. There is also information on the theory of operation, maintenance procedures, and ordering parts and supplies. This chapter includes general information that needs to be reviewed before servicing the PageWriter Touch cardiograph. Review the PageWriter Touch Cardiograph Instructions for Use, Edition 7 before servicing this device. This Service Manual assumes knowledge of all cardiograph controls and basic features. Before attempting to service the cardiograph, review the PageWriter Touch Cardiograph Instructions for Use, Edition 7 for software version C.01.02 and higher or Edition 6 for software version B.01.http://gillsandgeckos.com/userfiles/crain-812-super-saw-manual.xml Conventions Used in this Service Manual The Service Manual uses the following typographic conventions. Item How Displayed Menu item Button name Menu items and button names appear in a bold no-serif font. Keyboard keys Keyboard keys, such as Enter, or Tab, appear in italic font. Example: Touch Config. Example: Press Enter after typing the name. WARNING Warning statements describe conditions or actions that may result in a potentially serious outcome, adverse event, or a safety hazard. Failure to follow a Warning may result in death or serious injury to the user or to the patient. CAUTION Caution statements describe when special care is necessary for the safe and effective use of the product. Failure to follow a caution may result in minor to moderate personal injury or damage to the product or other property, a remote risk of more serious injury, or may cause environmental pollution. NOTE TIP Notes contain additional important information about a topic. A Tip contains suggested information on using a particular feature. Menu items and button names appear in bold no-serif font. Example: Touch the Config button. 1-2 PageWriter Touch Cardiograph Service Manual Page 16 Introduction Safety Summary Safety Summary Safety Symbols Marked on the Cardiograph Symbol Name Description Attention See PageWriter Touch Instructions for Use for information. Type CF ECG physio isolation is type CF, defibrillator proof. Suitable for all patient applications including direct cardiac application. System is in continuous operation. Alternating current Indicates that the cardiograph is receiving alternating voltages. Standby Pressing the button with this symbol on it puts the cardiograph into Standby (power saving mode). Equipotential grounding post Equipotential grounding post used for establishing common ground between instruments. Fuse Cardiograph contains a 1.5 amp (250V) time-delay fuse. Input The connector near this symbol receives an incoming signal.https://skazkina.com/ru/bose-wave-music-system-ii-manual Electrostatic Discharge Do not touch exposed pins. Touching exposed pins can cause electrostatic discharge which can damage the cardiograph. PIM (Patient Interface Module), Attention Attention, see PageWriter Touch Instructions for Use for information on PIM RJ-11 receptacle. Serial Number The number next to this symbol is the serial number of the cardiograph. Product model number The number next to this symbol is the product model number of the cardiograph Entry of liquids Cardiograph has ordinary protection against the entry of liquids. Entry of liquids The PIM (Patient Interface Module) is protected against splashing water. Water splashed against the PIM from any direction shall have no harmful effect. PageWriter Touch Cardiograph Service Manual 1-3 Page 17 Introduction Safety Summary Safety Symbols Marked on the Cardiograph Symbol Name Description Global Medical Device Nomenclature Code Global Medical Device Nomenclature Code is a 5-digit code providing a brief description of the device, as defined by EN ISO 15225. Safety Symbols Marked on the Cardiograph Packaging Symbol Description Keep dry. Ambient temperature range of 15 oC (59o F) to 35 oC (95o F) (non-condensing) for transport and storage. Atmospheric pressure range of 466 hPa to 1014 hPa for transport and storage. Relative humidity range of 25 to 80 (non-condensing) for transport and storage. Made from recycled materials. Fragile. Lithium ion battery. Do not dispose of in trash. Follow local regulations for disposing of as small chemical waste. This product consists of devices that may contain mercury, which must be recycled or disposed of in accordance with local, state, or federal laws. (Within this system, the backlight lamps in the monitor display contain mercury.http://impressionmexico.com/images/canon-rebel-t2i-manual-settings.pdf) 1-4 PageWriter Touch Cardiograph Service Manual Page 18 Introduction Important Patient and Safety Information Safety Symbols Marked on the Cardiograph Packaging Symbol Description Dispose of in accordance with the requirements of your country. Important Patient and Safety Information The PageWriter Touch cardiograph isolates all connections to the patient from electrical ground and all other conductive circuits in the cardiograph. This reduces the possibility of hazardous currents passing from the cardiograph through the patient’s heart to ground. WARNING Failure to follow these warnings could affect both patient and operator safety. WARNING Do not connect the modem card to a phone line when the cardiograph is connected to a patient. WARNING Do not touch accessible connector pins and the patient simultaneously. Electrical shock hazard. Keep cardiograph, Patient Interface Module (PIM) and all cardiograph accessories away from liquids. Do not immerse the cardiograph, PIM, or other accessories in any liquids. WARNING When using additional peripheral equipment powered from an electrical source other than the cardiograph, the combination is considered to be a medical system. It is the responsibility of the operator to comply with IEC 60601-1-1 and test the medical system according to the requirements. For additional information contact Philips Medical Systems. WARNING Do not use non-medical peripherals within 6 feet of a patient unless the non-medical peripherals receive power from the cardiograph or from an isolation transformer that meets medical safety standards. WARNING The Welsh bulb electrodes (available as an accessory for the cardiograph) do not meet the requirements of IEC 60601-2-25 for defibrillation recovery time, and cannot be reliably used for patient diagnosis following defibrillation. PageWriter Touch Cardiograph Service Manual 1-5 Page 19 Introduction 1-6 Important Patient and Safety Information. When operating the cardiograph on AC power, ensure that the cardiograph and all other electrical equipment connected to or near the patient are effectively grounded. ? Use only grounded power cords (three-wire power cords with grounded plugs) and grounded electrical outlets. Never adapt a grounded plug to fit an ungrounded outlet by removing the ground prong or ground clip. If an ungrounded plug adapter is required, use a ground strap to connect the equipotential post (rear of the cardiograph, see page 1-13) to the power source ground. Use the equipotential post when redundant earth ground is necessary according to IEC 60601-1. ? If a safe ground connection is not ensured, operate the cardiograph on battery power only. ? The use of equipment that applies high frequency voltages to the patient (including electrosurgical equipment and some respiration transducers) is not supported and may produce undesired results. ? Periodically inspect the patient data cable, lead wires, and AC power cord for any worn or cracked insulation. ? Keep the patient data cable away from power cords and any other electrical equipment. Failure to do so can result in AC power line frequency interference on the ECG trace. ? The Philips Medical Systems patient data cable (supplied with cardiograph) is an integral part of the cardiograph safety features. Use of any other patient data cable may compromise defibrillation protection and degrade cardiograph performance. ? Only qualified personnel may service the cardiograph or may open the cardiograph housing to access internal cardiograph components. Do not open any covers on the cardiograph. There are no internal cardiograph components that are serviced by the operator. ? Do not use this cardiograph near flammable anesthetics. It is not intended for use in explosive environments or in operating rooms. ? The use of the analog ECG output signal port (not supported on cardiograph, see page 1-13) should not be used when critical synchronization timing is required. ? Do not touch the patient, patient data cable, or cardiograph during defibrillation. Death or injury may occur from the electrical shock delivered by the defibrillator. ? Ensure that the electrodes or lead wires do not come in contact with any other conductive materials (including earth-grounded materials) especially when connecting or disconnecting electrodes to or from a patient. ? Connecting multiple cardiographs to the same patient may pose a safety hazard due to the summation of leakage currents. Any combination of instruments should be evaluated by local safety personnel before being put into service. ? Do not pull on the paper while an ECG report is being printed. This can cause distortion of the waveform and can lead to potential misdiagnosis. ? Do not connect any equipment to the cardiograph RS-232 port that does not meet medical safety requirements and that has not been evaluated by local safety personnel. PageWriter Touch Cardiograph Service Manual Page 20 Introduction Important Patient and Safety Information. Equipment connected to the cardiograph RS-232 port can cause ground leakage currents exceeding the maximum specified in IEC 60601-1 safety standards. ? Do not connect any equipment to the cardiograph RS-232 port if a patient is connected to the cardiograph. ? Only use the Philips Medical Systems AC power cord supplied with the cardiograph. Periodically inspect the AC power cord and AC power connector (rear of cardiograph, see page 1-13) to ensure that both are in a safe and operable condition. If the AC power cord or AC power connector is not in a safe or operable condition, operate the cardiograph on battery power and contact Philips Medical Systems for service. ? The cardiograph has been safety tested with the recommended accessories, peripherals, and leads, and no hazard was found when the cardiograph is operated with cardiac pacemakers or other stimulators. ? Do not connect any equipment or accessories to the cardiograph that are not approved by Philips Medical Systems or that are not IEC 60601-1 approved. The operation or use of non-approved equipment or accessories with the cardiograph is not tested or supported, and cardiograph operation and safety are not guaranteed. ? Only install Philips Medical Systems software on the cardiograph. The installation or use of software not approved by Philips Medical Systems is strictly prohibited and cardiograph safety and performance are not guaranteed. ? Only use Philips Medical Systems replacement parts and supplies with the cardiograph. The use of non-approved replacement parts and supplies with the cardiograph is strictly prohibited. Cardiograph safety and performance are not guaranteed when non-approved replacement parts and supplies are used with the cardiograph. ? Manual measurements of ECG intervals and magnitudes should be performed on printed ECG reports only. Do not make manual measurements of ECG intervals and magnitudes on the touchscreen display since these ECG representations are scaled. ? Only use patient electrodes that are approved by Philips Medical Systems. The use of nonapproved patient electrodes may degrade cardiograph performance. ? The Philips Medical Systems warranty is applicable only if you use Philips Medical Systems approved accessories and replacement parts. See “Supplies and Ordering Information” on page 1-24 for more information. ? For information on the standard IEC 60601-2-51, please go to the Philips InCenter web site (incenter.medical.philips.com). For information on using the Philips InCenter site, see page 129. ? Always put the cardiograph in Standby before replacing the Patient Interface Module (PIM). Do not change the PIM while the cardiograph is in active use. PageWriter Touch Cardiograph Service Manual 1-7 Page 21 Introduction The PageWriter Touch Cardiograph The PageWriter Touch Cardiograph This Philips product is intended to be used and operated only in accordance with the safety procedures and operating instructions provided in this Instructions for Use, and for the purposes for which it was designed. The purposes for which the product is intended are provided below. However, nothing stated in this Instructions for Use reduces the responsibility of the user for sound clinical judgment and best clinical procedures. Intended Use The intended use of the cardiograph is to acquire multi-channel ECG signals from adult and pediatric patients from body surface ECG electrodes and to record, display, analyze, and store these ECG signals for review by the user. The cardiograph is to be used in healthcare facilities by trained healthcare professionals. Analysis of the ECG signals is accomplished with algorithms that provide measurements, data presentations, graphical presentations, and interpretations for review by the user. The interpreted ECG with measurements and interpretive statements is offered to the clinician on an advisory basis only. It is to be used in conjunction with the clinician's knowledge of the patient, the results of the physical examination, the ECG tracings, and other clinical findings. A qualified physician is asked to overread and validate (or change) the computer-generated ECG interpretation. Indications for Use The cardiograph is to be used where the clinician decides to evaluate the electrocardiogram of adult and pediatric patients as part of decisions regarding possible diagnosis, potential treatment, effectiveness of treatment, or to rule out causes for symptoms. The Philips 12-Lead Algorithm The PageWriter Touch Cardiograph software uses the Philips 12-Lead Algorithm. The algorithm in the software analyzes the morphology and rhythm on each of the 12 leads and summarizes the results. The set of summarized measurements is then analyzed by the clinically-proven ECG Analysis Program. 12-lead reports may include or exclude ECG measurements, reasons, or analysis statements. Intended Use The intended use of the Philips 12-Lead Algorithm is to analyze multi-channel ECG signals from adult and pediatric patients with algorithms that provide measurements, data presentations, graphical presentations, and interpretations for review by the user. The interpreted ECG with measurements and interpretive statements is offered to the clinician on an advisory basis only. It is to be used in conjunction with the clinician's knowledge of the patient, the results of the physical examination, the ECG tracings, and other clinical findings. A qualified physician is asked to overread and validate (or change) the computer-generated ECG interpretation. 1-8 PageWriter Touch Cardiograph Service Manual Page 22 Introduction Cardiograph Features Indications for Use The Philips 12-Lead Algorithm is to be used where the clinician decides to evaluate the electrocardiogram of adult and pediatric patients as part of decisions regarding possible diagnosis, potential treatment, effectiveness of treatment, or to rule out causes for symptoms. Cardiograph Features The PageWriter Touch cardiograph is one of the most advanced cardiographs. It offers touch screen operation and numerous additional features making it ideal for high-volume environments. The PageWriter Touch cardiograph is also well suited for hospitals requiring speed and accuracy to process large volumes of ECGs daily. The PageWriter Touch cardiograph consists of an electrocardiograph with remote digital patient module and an optional cart. Features The features of the PageWriter Touch cardiograph include. Battery or AC operation. Remote digital acquisition module with replaceable patient leads with the capability for up to 12 leads (software version B.01), or up to 16 leads (software version C.01.02 and higher) ? Three 15 and 16-lead options are available with software version C.01.02 and higher for both adult and pediatric application ? 15-inch color liquid crystal touch screen display. Graphical representation of a human torso displaying leads that are loose or not connected. Data transmission between the cardiograph and a TraceMasterVue ECG Management system in XML format via modem, LAN, WLAN, diskette, or optional PC (PCMCIA) storage card, or USB memory stick. Software version C.01.02 and higher supports the export of ECG data in XML version 1.03, or XML version 1.04 ? Optional cart with convenient storage areas for supplies. Software version B.01, and C.01.02 and higher, support bidirectional orders download and search capability with an OrderVue order handling system. Software version B.01, and C.01.02 and higher, support algorithm version PH080A and PH090A; algorithm version PH090A includes new enhancements and features including heightened detection of atrial arrhythmia, the ability to suppress statements that indicate a borderline or otherwise normal condition, lead reversal detection feature, ECG warning statements when a life threatening cardiac event is detected, and the ability to print Fridericia rate corrected QT interval and RR measurements on the ECG report PageWriter Touch Cardiograph Service Manual 1-9 Page 23 Introduction PageWriter Touch Cardiograph Components. Time Sychronization feature that is used with a TraceMasterVue ECG Management System (version B.01 and higher). Use of this feature helps to ensure the accuracy of the displayed time on the cardiograph by regularly calibrating it with a configured TraceMasterVue Remote Site PageWriter Touch Cardiograph Components The following sections illustrate the components and connection ports on the cardiograph and the Patient Interface Module (PIM). Figures 1-1, 1-2, and 1-3 on the following pages show front, side, and rear views of the PageWriter Touch cardiograph. Do not plug a telephone connector into the PIM RJ-11 receptacle. Sign in Forgot Password. My Bench Close Sign In Not A Member. Sign Up Join MedWrench OK name type Receive Summary Emails. A high-resolution 15-inch touch screen clearly displays 10 seconds of all 12 leads, color-coded for signal quality. Preview the full report waveform and interpretation before printing to save time and paper. Wireless communication simplifies life, allowing you to quickly download orders and send data to your EKG management system all in record time. Easy, Fast, 12-Lead EKGs for Hospitals Large or Small. FORUMS View All (6) Ask a New Question 1 Reply -H A v d Velde 7 months ago 7 months ago password setup I need password for setup Philips page writer touchHowever no one here remembers the password. I tried the hard reset procedure but it still wants a password and the few i tried do not work like 0000, service, biomed. Also in the reset procedure it says to remove the card from the rear but this machine does not have a card. Anyway any help would be appreciated Reply 1 Reply -HRS 3 years ago 3 years ago PageWriter What is the year of manufacture of the TC10 and TC20? Has the TC20 been discontinued.By continuing to browse the site you are agreeing to our use of cookies. Please review our Privacy Policy for more details. All Rights Reserved. Sign in Forgot Password. My Bench Close Sign In Not A Member. Sign Up Join MedWrench OK name type Receive Summary Emails.However no one here remembers the password. I tried the hard reset procedure but it still wants a password and the few i tried do not work like 0000, service, biomed. Also in the reset procedure it says to remove the card from the rear but this machine does not have a card. Anyway any help would be appreciated Report Post Biomed2015 Fri Feb 15 2019 Reply from Biomed2015 Try Athena as the password. Don't forget the cap lock is on by default. Report Post BrentS Mon Feb 18 2019 Reply from BrentS Not sure if this will help, but I found this information listed in the service manual. The last section may be of help. You can change the access code to any combination of four (4) numeric digits. If you lose or forget the access code, contact the Philips Response Center. Calibrate Batteries Battery calibration from the Service Utility screen is not supported. Battery calibration can be initiated from the Maintenance screen in Configuration. For details, see “Battery Maintenance and Care” on page 3-6. Refresh Data The information displayed in the Service Utility does not refresh automatically. To refresh the Service Utility screen: AX Touch Refresh to display the latest data. Print Status Allows you to print the information displayed in the Service Utility. To print the contents of the Service Utility screen: AX Touch Print Status. If desired, type the tester name, date, and time in the Tester Info field for inclusion on the report. Restart Unit Touch Restart Unit to exit the Service Utility and reset the cardiograph. You must always reset the cardiograph after exiting the Service Utility. NOTE Entering the Service Utility requires a full reboot of cardiograph. Any unsaved patient data will be lost. 2 Perform a soft reset by pressing the Reset button adjacent to the USB connector on the rear panel of the cardiograph. After approximately 40 seconds, the PageWriter Touch software ID screen appears, followed by an audible beep. 3 Quickly, while the splash screen is displayed, hold down the right CTRL and SHIFT keys together and tap the touch screen. An Access Code window appears. The factory default code is 0000 (zero). 5 Type explorer at the command prompt. To exit the Windows CE desktop: Press the Reset button located in the rear of the cardiograph.By continuing to browse the site you are agreeing to our use of cookies. Please review our Privacy Policy for more details. All Rights Reserved. And by having access to our ebooks online or by storing it on your computer, you have convenient answers with Philips Pagewriter Touch User Manual. To get started finding Philips Pagewriter Touch User Manual, you are right to find our website which has a comprehensive collection of manuals listed. Our library is the biggest of these that have literally hundreds of thousands of different products represented. I get my most wanted eBook Many thanks If there is a survey it only takes 5 minutes, try any survey which works for you. Notice Notice 0. The information in this document is subject to change without notice. Hewlett-Packard makes no warranty of any kind with regard to this material, including, but not limited to, the implied warranties of merchantability and fitness for a particular purpose. Hewlett-Packard shall not be liable for errors contained herein or for incidental or consequential damages in connection with the furnishing, performance, or use of this material. This document contains or refers to proprietary information which is protected by copyright. All rights are reserved. No part of this document may be photocopied, reproduced, or translated to another language without the prior written consent of Hewlett- Packard Company.) Notice Notice 0. The information in this document is subject to change without notice. Hewlett-Packard makes no warranty of any kind with regard to this material, including, but not limited to, the implied warranties of merchantability and fitness for a particular purpose. Hewlett-Packard shall not be liable for errors contained herein or for incidental or consequential damages in connection with the furnishing, performance, or use of this material. This document contains or refers to proprietary information which is protected by copyright. All rights are reserved. No part of this document may be photocopied, reproduced, or translated to another language without the prior written consent of Hewlett- Packard Company.) 2 Responsibility of the Manufacturer Hewlett-Packard only considers itself responsible for any effects on safety, reliability and performance of the equipment if all the following are true: Assembly operations, extensions, re-adjustments, modifications or repairs are done by persons authorized by Hewlett-Packard. The electrical installation of the relevant room complies with the IEC or national require- ments. The instrument is used according to the instructions for use presented in this Manual. WARNING As with all electronic equipment, radio frequency interference between this cardiograph and any existing RF transmitting or receiving equipment at the installation site, including electrosurgical equipment, should be evaluated carefully and any limitations noted before the equipment is placed in Service. Monitoring during electrosurgery should not be attempted and monitoring electrodes should be removed from the patient to preclude the possibility of burns. 3 Radio frequency generation from electrosurgical equipment and close proximity transmitters may seriously degrade cardiograph performance. Hewlett- Packard assumes no liability for failures resulting from RF interference between HP medical electronics and any radio frequency generating equipment at levels exceeding those established by applicable standards.