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DIGITAL MONOCHROME PRINTER MODEL P95DW P95DE OPERATION MANUAL THIS OPERATION MANUAL IS IMPORTANT TO YOU. PLEASE READ IT BEFORE USING YOUR DIGITAL MONOCHROME PRINTER. DIGITAL MONOCHROME PRINTER This digital monochrome printer complies with the requirements of the EC Directive 93/42/EEC.

FOR THE MODEL P91DW(UB) ONLY WARNING: In the USA or Canada, use the AC power cord according to the recommendations as below, in order to comply with UL60601-1 and CAN/CSA C22.2 No. 601.1. Case 1. Connect to the 120V receptacle of the room or the host equipment. The AC power cord should be UL or CSA approved and consist of type SJT, size 16 or 18AWG, length 2.5m or shorter cord with IEC60320-1/C13 type, 125V 10A or higher rating connector and NEMA 5-15 type, 125V 10A or higher rating, Hospital Grade plug. Case 2. Connect to the 230V receptacle of the room or the host equipment. The AC power cord should be UL or CSA approved and consist of type SJT, size 16 or 18AWG, length 2.5m or shorter cord with IEC60320-1/C13 type, 250V 10A or higher rating connector and NEMA 6-15 type, 250V 10A or higher rating, Hospital Grade plug. CAUTION: Changes or modifications not expressly approved by the party responsible for compliance could void the user’s authority to operate the equipment. 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 harm- ful interference when the equipment is operated in a commercial environ- ment. 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 interfer- ence at his or her own expense. Information: This class A digital apparatus complies with Canadian ICES-003. "CLASSIFIED BY UNDERWRITERS LABORATORIES INC.® WITH RESPECT TO ELECTRIC SHOCK, FIRE AND MECHANICAL HAZARDS ONLY IN ACCORDANCE WITH UL60601-1 AND CAN/CSA C22.2 No. 601.1"

Indications according to IEC60601-1 1. Functions and intended usage of this product This product receives signals from diagnostic imaging equipment or a personal computer, and automatically prints and ejects the received image data on the thermal paper. 2. Classiﬁ cation of this product • According to the type of protection against electric shock: Equipment energized from an external electrical power source, Class I equipment • According to the degree of protection of the applied part against electric shock: - (No applied part) • According to the degree of protection against harmful ingress of water: Ordinary equipment (Enclosed equipment without protection against ingress of water) • According to the degree of safety of application in the presence of a ﬂ ammable anesthetic mixture with air or with oxygen or nitrous oxide: Equipment not suitable for use in the presence of a ﬂ ammable anesthetic mixture with air or with oxygen or nitrous oxide • According to the mode of operation: Continuous operation with intermittent loading 3. Follow the applicable laws and regulations in your country or region or the hospital rules when disposing of this product or the accessories or consumables thereof. DANGER: EXPLOSION HAZARD. DO NOT USE IN THE PRESENCE OF FLAMMABLE ANESTHETICS.

CAUTION: RISK OF ELECTRIC SHOCK DO NOT OPEN. TO REDUCE THE RISK OF ELECTRIC SHOCK, DO NOT REMOVE COVER (OR BACK). NO USER-SERVICEABLE PARTS INSIDE. REFER SERVICING TO QUALIFIED SERVICE PERSONNEL. The lightning ﬂ ash with arrowhead symbol, within an equilateral triangle, is intended to alert the user to the presence of uninsulated "dangerous voltage" within the product's enclosure that may be of sufﬁ cient magnitude to constitute a risk of electric shock. The exclamation point within an equilateral triangle is intended to alert the user to the presence of important operating and maintenance (servicing) instructions in the literature accompanying the appliance. The “Caution, hot surface” symbol indicates that the marked item may be hot and should not be touched. The “Nonionizing radiation” symbol The “OFF/ON” symbol indicates connection to or disconnection from the mains, at least for mains switches. The “Equipotentiality” symbol identiﬁ es the terminals connected each other. The potential of various parts of equipment or of a system is equalized. The “Alternating current” symbol indicates that the equipment is suitable for alternating current only. When you dispose of the unit or accessories, you must obey the law in the relative area or country and/or regulation in the relative hospital. : Manufactured on : to be combined with date code YYYY-MM : Manufacturers Identiﬁ cation (name address) : Serial number : Authorised representative in the European Community

WARNING: Install and use this appliance in accordance with the operation manual for safety and EMC (Electromagnetic Compatibility). If it is not installed and used in accordance with the operation manual, it may cause interference to other equipment and/or other risk. To prevent ﬁ re or shock hazard, do not expose this appliance to rain or moisture. This appliance must be earthed. In Europe, use the AC power cord according to the recommendations as below. Connect to the 230 V receptacle of the room or the host equipment. The AC power cord should be VDE approved and consist of core size 0.75 mm2 or bigger, length 2.5 m or shorter cord with IEC60320-1/C13 type, 250 V 10 A or higher rating connector and CEE(7)VII type, 250 V 10 A or higher rating plug. Use the USB cable according to the recommendations as below, in order to comply with EN60601-1-2. The USB cable with appropriate plug should be 2 m long or shorter, comply with USB 2.0 standard High speed requirements and USB IF (USB Implementers Forum) approved. This product is to be employed with medical equipment, just for reference purpose, not for medical diagnostic purpose. WARNING: The socket outlet shall be installed near the equipment and shall be easily ac- cessible. Note: This symbol mark is for EU countries only. This symbol mark is according to the directive 2002/96/EC Article 10 Information for users and Annex IV. Your MITSUBISHI ELECTRIC product is designed and manufactured with high quality materials and components which can be recycled and reused. This symbol means that electrical and electronic equipment, at their end-of-life, should be disposed of separately from your household waste. Please, dispose of this equipment at your local community waste collection/recycling centre. In the European Union there are separate collection systems for used electrical and electronic product. Please, help us to conserve the environment we live in!

INSTRUCTIONS FOR MEDICAL USE MEDICAL ELECTRICAL EQUIPMENT needs special precautions regarding EMC and needs to be installed and put into service according to the EMC information provided in the AC- COMPANYING DOCUMENTS. Portable and mobile RF communications equipment can affect MEDICAL ELECTRICAL EQUIPMENT. Technical description List of all cables and maximum length of the cable and other ACCECCORIES Maximum length Reference page in this operation manual AC power cord 2.5 m This page, the previous pages for safety and page 25 for accessories USB cable 2 m This page and the previous pages for safety Thermal paper Page 3 for thermal paper, Page 25 for accessories WARNING: The use of ACCESSORIES and cables other than those speciﬁ ed, with the exception of ca- bles sold by the manufacturer of the Model P95DW/P95DE as replacement parts for internal components, may result in increased EMISSIONS or decreased IMMUNITY of the Model P95DW/P95DE. WARNING: The Model P95DW/P95DE should not be used adjacent to or stacked with other equipment and that if adjacent or stacked use is necessary, the Model P95DW/P95DE should be ob- served to verify normal operation in the conﬁ guration in which it will be used.

Guidance and manufacturer's declaration - electromagnetic emissions The Model P95DW/P95DE is intended for use in the electromagnetic environment specified below. The customer or user of the Model P95DW/P95DE should assure that it is used in such an environment. Emissions test RF emissions CISPR 11/EN 55011 Compliance Group 1 RF emissions CISPR 11/EN 55011 Harmonic emissions IEC/EN 61000-3-2 Voltage fluctuations/ flicker emissions IEC/EN 61000-3-3 Class B Class A Complies Electromagnetic environment - guidance The Model P95DW/P95DE uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause interference in nearby electronic equipment. The Model P95DW/P95DE is suitable for use in all establishments, including domestic establishments and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes. Guidance and manufacturer's declaration - electromagnetic immunity The Model P95DW/P95DE is intended for use in the electromagnetic environment specified below. The customer or user of the Model P95DW/P95DE should assure that it is used in such an environment. IEC/EN 60601 test level ±6 kV contact ±8 kV air Compliance level ±6 kV contact ±8 kV air ±2 kV for power supply lines ±1 kV for input /output lines ±1 kV line(s) to line(s) ±2 kV line(s) to earth ±2 kV for power supply lines ±1 kV for input /output lines ±1 kV line(s) to line(s) ±2 kV line(s) to earth Electromagnetic environment - guidance Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%. Mains power quality should be that of a typical commercial or hospital environment. Mains power quality should be that of a typical commercial or hospital environment. Immunity test Electrostatic discharge (ESD) IEC/EN 61000-4-2 Electrical fast transient/burst IEC/EN 61000-4-4 Surge IEC/EN 61000-4-5 Voltage dips, short interruptions and voltage variations on power supply input lines IEC/EN 61000-4-11 Mains power quality should be that of a typical commercial or hospital environment. If the user of the Model P95DW/P95DE requires continued operation during power mains interruptions, it is recommended that the Model P95DW/P95DE be powered from an uninterruptible power supply or a battery. < 5% UT (> 95% dip in UT) for 0.5 cycle 40% UT (60% dip in UT) for 5 cycles 70% UT (30% dip in UT) for 25 cycles < 5% UT (> 95% dip in UT) for 5 sec. 3 A/m < 5% UT (> 95% dip in UT) for 0.5 cycle 40% UT (60% dip in UT) for 5 cycles 70% UT (30% dip in UT) for 25 cycles < 5% UT (> 95% dip in UT) for 5 sec. 3 A/m Power frequency (50/60 Hz) magnetic field IEC/EN 61000-4-8 NOTE: UT is the a.c. mains voltage prior to application of the test level. Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment.

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