DIGITALMONOCHROMEPRINTER
MODEL
P95DW
P95DE
OPERATION MANUAL
THISOPERATIONMANUALISIMPORTANT
TO YOU.
PLEASEREADITBEFOREUSINGYOUR
DIGITALMONOCHROMEPRINTER.
DIGITALMONOCHROME 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 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 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. Classification 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 flammable anesthetic mixture with air or with oxygen or nitrous oxide: Equipment not suitable for use in the presence of a flammable 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 flash 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 sufficient 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 identifies 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 Identification (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 fire 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 accessible.
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
<according to the Medical Safety/EMC standard IEC/EN 60601-1-2>
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 ACCOMPANYING 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
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Maximum length |
Reference page in this operation manual |
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AC power cord |
2.5 m |
This page, the previous pages for safety and page 25 |
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for accessories |
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USB cable |
2 m |
This page and the previous pages for safety |
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Thermal paper |
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Page 3 for thermal paper, Page 25 for accessories |
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WARNING:
The use of ACCESSORIES and cables other than those specified, with the exception of cables 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 observed to verify normal operation in the configuration 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.
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Emissions test |
Compliance |
Electromagnetic environment - guidance |
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RF emissions |
Group 1 |
The Model P95DW/P95DE uses RF energy only for its |
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CISPR 11/EN 55011 |
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internal function. Therefore, its RF emissions are very |
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low and are not likely to cause interference in nearby |
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electronic equipment. |
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RF emissions |
Class B |
The Model P95DW/P95DE is suitable for use in all |
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CISPR 11/EN 55011 |
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establishments, including domestic establishments |
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Harmonic emissions |
Class A |
and those directly connected to the public low-voltage |
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IEC/EN 61000-3-2 |
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power supply network that supplies buildings used for |
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Voltage fluctuations/ |
Complies |
domestic purposes. |
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flicker emissions |
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IEC/EN 61000-3-3 |
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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.
Immunity test |
IEC/EN 60601 |
Compliance |
Electromagnetic environment - guidance |
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test level |
level |
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Electrostatic |
±6 kV contact |
±6 kV contact |
Floors should be wood, concrete or |
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discharge (ESD) |
±8 kV air |
±8 kV air |
ceramic tile. If floors are covered with |
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IEC/EN 61000-4-2 |
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synthetic material, the relative humidity |
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should be at least 30%. |
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Electrical fast |
±2 kV for power |
±2 kV for power |
Mains power quality should be that of a |
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transient/burst |
supply lines |
supply lines |
typical commercial or hospital |
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IEC/EN 61000-4-4 |
±1 kV for input |
±1 kV for input |
environment. |
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/output lines |
/output lines |
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Surge |
±1 kV line(s) to |
±1 kV line(s) to |
Mains power quality should be that of a |
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IEC/EN 61000-4-5 |
line(s) |
line(s) |
typical commercial or hospital |
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±2 kV line(s) to |
±2 kV line(s) to |
environment. |
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earth |
earth |
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Voltage dips, short |
< 5% UT |
< 5% UT |
Mains power quality should be that of a |
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interruptions and |
(> 95% dip in UT) |
(> 95% dip in UT) |
typical commercial or hospital |
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voltage variations |
for 0.5 cycle |
for 0.5 cycle |
environment. If the user of the Model |
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on power supply |
P95DW/P95DE requires continued |
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40% UT |
40% UT |
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input lines |
operation during power mains |
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(60% dip in UT) |
(60% dip in UT) |
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IEC/EN 61000-4-11 |
interruptions, it is recommended that the |
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for 5 cycles |
for 5 cycles |
Model P95DW/P95DE be powered from |
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70% UT |
70% UT |
an uninterruptible power supply or a |
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(30% dip in UT) |
(30% dip in UT) |
battery. |
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for 25 cycles |
for 25 cycles |
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< 5% UT |
< 5% UT |
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(> 95% dip in UT) |
(> 95% dip in UT) |
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for 5 sec. |
for 5 sec. |
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Power frequency |
3 A/m |
3 A/m |
Power frequency magnetic fields should |
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(50/60 Hz) |
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be at levels characteristic of a typical |
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magnetic field |
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location in a typical commercial or |
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IEC/EN 61000-4-8 |
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hospital environment. |
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NOTE: UT is the a.c. mains voltage prior to application of the test level.
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.
Immunity test |
IEC/EN 60601 |
Compliance |
Electromagnetic environment - guidance |
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test level |
level |
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Portable and mobile RF communications |
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equipment should be used no closer to |
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any part of the Model P95DW/P95DE, |
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including cables, than the recommended |
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separation distance calculated from the |
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equation applicable to the frequency of |
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the transmitter. |
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Recommended separation distance |
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Conducted RF |
3 Vrms |
3 Vrms |
d=1.2√P |
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IEC/EN 61000-4-6 |
150 kHz to 80 |
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MHz |
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Radiated RF |
3 V/m |
3 V/m |
d=1.2√P 80 MHz to 800 MHz |
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IEC/EN 61000-4-3 |
80 MHz to 2.5 |
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d=2.3√P 800 MHz to 2.5 GHz |
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GHz |
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where P is the maximum output power |
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rating of the transmitter in watts (W) |
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according to the transmitter manufacturer |
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and d is the recommended separation |
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distance in meters (m). |
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Field strengths from fixed RF |
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transmitters, as determined by an |
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electromagnetic site survey,a should be |
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less than the compliance level in each |
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frequency range.b |
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Interference may occur in the vicinity of |
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equipment marked with the following |
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symbol: |
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NOTE1. At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE2. These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.
aField strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the Model P95DW/P95DE is used exceeds the applicable RF compliance level above, the Model P95DW/P95DE should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the Model P95DW/P95DE.
bOver the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
Recommended separation distances between
portable and mobile RF communications equipment and the Model P95DW/P95DE
The Model P95DW/P95DE is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the Model P95DW/P95DE can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the Model P95DW/P95DE as recommended below, according to the maximum output power of the communications equipment.
Rated maximum output |
Separation distance according to frequency of transmitter |
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power of transmitter |
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m |
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W |
150 kHz to 80 MHz |
80 MHz to 800 MHz |
800 MHz to 2.5 GHz |
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d=1.2√P |
d=1.2√P |
d=2.3√P |
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0.01 |
0.12 |
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0.12 |
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0.23 |
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0.1 |
0.38 |
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0.38 |
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0.73 |
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1 |
1.2 |
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1.2 |
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2.3 |
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10 |
3.8 |
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3.8 |
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7.3 |
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100 |
12 |
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12 |
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23 |
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For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
NOTE1. At 80 MHz and 800 MHz, the separation distance for higher frequency range applies.
NOTE2. These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.
Safety Notices for use in combination with other devices
1.All the equipments connected to this unit shall be certified according to Standard IEC60601-1, IEC60950-1, IEC60065 or other IEC/ISO Standards applicable to the equipments.
2.When this unit is used together with other equipment in the patient area*, the equipment shall be either powered by an isolation transformer or connected via an additional protective earth terminal to system ground unless it is certified according to Standard IEC60601-1.
*Patient Area
R1.5m
3. The leakage current could increase when connected to other equipment.
1 
CONTENTS
CONTENTS.................................................................. |
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1 |
PRECAUTIONS ..................................................... |
2 - 5 |
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UNPACKING................................................................ |
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6 |
FEATURES AND FUNCTIONS............................... |
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7 - 8 |
Front Panel .......................................................................................... |
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7 |
Rear Panel ........................................................................................... |
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8 |
INSTALLATION OF PAPER ................................. |
9 |
- 10 |
EXAMPLE OF CONNECTION.................................... |
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11 |
PRINTING ........................................................... |
12 |
- 13 |
ADJUSTMENT OF PRINT PICTURE ................. |
14 |
- 16 |
SETTING FUNCTION MODE ............................. |
17 |
- 18 |
ERROR DISPLAY ............................................... |
19 |
- 21 |
STATUS AND MODES............................................... |
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22 |
USE OF CLEANING PAPER ..................................... |
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23 |
MAINTENANCE......................................................... |
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24 |
SPECIFICATIONS ..................................................... |
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25 |
1
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