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Фрагмент инструкции
Important ............................................... 1 1.1 Power adapter safety Information .......1 1.2 EMC information ..........................................2 1.3 Safety precautions and maintenance .6 1.4 Notational Descriptions ............................7 1.5 Disposal of product and packing material ...............................................................8 1.6 AntiMicrobial housing .................................9 2. Setting up the monitor .....................10 2.1 Installation ......................................................10 2.2 Operating the monitor ...........................12 2.3 Remove the Base Assembly for VESA Mounting .........................................................14 3. Image Optimization ...........................15 3.1 Smar tImageCLINIC .........................................15 3.2 Philips Smar tControl Premium ..........16 3.3 Smar tDesktop Guide ..............................23 4. PowerSensor™ ..................................28 5. Te..hni..al Spe..i....ations ....................29 5.1 Resolution & Preset Modes .................31 6. Power Management ...........................32 7. Regulatory Information .....................33 8. Customer care and warranty ..........40 8.1 Philips’ Flat Panel Monitors Pixel Defect Policy .................................................40 8.2 Customer Care & Warranty ...............42 9. Troubleshooting & FAQs ..................46 9.1 Troubleshooting ..........................................46 9.2 Smar tControl Premium FAQs ...........47 9.3 General FAQs ..............................................48 9.4 Clinical FAQ ..................................................50 1. Important 1. Important 1. Important The monitor is intended for use with Medical Equipment to display alpha, numerical and graphical data.The subject equipment Philips monitor is powered by an external recognized AC/DC adaptor. (IEC/EN60601-1). 1.1 Power adapter safety Information Power adapter This adapter (Manufacture: Philips, Model: PMP60-13-1-HJ-S) is a forming par t of the medical device. The connection of external equipments External equipment intended for connection to signal input/output or other connectors, shall comply with relevant UL / IEC standard (e.g. UL 60950 for IT equipment, UL 60601-1 and ANSI/AAMI ES60601-1 / IEC 60601 series for systems – shall comply with the standard IEC 60601-1-1, Safety requirements for medical electrical systems. Equipment not complying with MOPP of ANSI/AAMI ES60601-1 shall be .............................................................................................. in the standard. Disconnecting Device The mains plug or appliance coupler is used as the disconnect device, the disconnect device shall remain readily operable. Always completely disconnect the power cord set from your product whenever you are working or cleaning on it. Do not make connections while the power is on, because a sudden rush of power can damage sensitive electronic components. Classi..cation .. Degree of protection against the ingress of water : IPX0 .. Equipment not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen or nitrous oxide. (Non AP or APG Categor y) .. Mode of operation: Continuous .. Type of protection against electric shock: Class I ME Equipment .. No Applied par t. Shutdown Procedure We strongly recommended that you should shut down the system before you star t to clean any single components. Please follow the steps below. .. Close all application programs .. Close operating software .. Turn off power switch .. Disconnect power cord set .. Remove all devices Safety Symbol Description The following safety symbols are the fur ther explanations for your reference. Medical component W............................................................................ mechanical hazards only in accordance with ANSI/AAMI ES60601-1, and CAN/ CSA C22.2 NO. 60601-1 Attention, consult ACCOMPANYING DOCUMENTS. Type of Current- AC Dircet Current European Community Approval, The monitor complies with the 93/42/ EEC and 2007/47/EC and conforms to the applicable following standards: EN60601-1, EN 60601-1-2, EN 610003- 2 and EN 61000-3-3. TUV Type Testing Approval, The monitor complies with the EN60601-1 and IEC60601-1 of European Standards. Power "ON" Power "OFF" Medical Equipment With respect to ...................................................................... hazards only in accordance with ANSI/ AAMI ES 60601-1:2005, and CAN/ CSA C22.2 NO.60601-1:2008 Note .. .. Caution: Use suitable mounting apparatus to avoid risk of injur y. Use a power cord that matches the voltage of the power outlet, which has been 1 1. Important 1. Important approved and complies with the safety .. Make sure user does not contact SIP/SOPs standards of your par ticular countr y. and the patient at the same time. 1.2 EMC information Guidance and manufacturer’s declaration – electromagnetic emissions – for all ...
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