Sony LMD-X2705MD Manual
Read below đź“– the manual in Italian for Sony LMD-X2705MD (38 pages) in the Monitor category. This guide has been helpful for 21 people and has been rated 4.5 stars on average by 2 users
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4-747-116-17(2)
LCD Monitor
Instructions for Use
Before operating the unit, please read this manual thoroughly
and retain it for future reference.
LMD-X2705MD
LMD-X2700MD
© 2019 Sony Corporation
2024-04
2
Indications for Use/Intended Use
The LCD Monitor is intended to provide 4K 2D color
video displays of images from endoscopic/
laparoscopic camera systems and other
compatible medical imaging systems.
The LCD Monitor is a widescreen, high-definition,
me
dical grade monitor for real-time use during
minimally invasive surgical procedures and is
suitable for use in hospital operating rooms,
surgical centers, clinics, doctors’ offices and
similar medical environments.
Notes
• This equipment is for medical professionals.
• This equipment is intended for use in medical
e
nvironments, such as doctors’ offices,
examination rooms, and operating rooms.
To reduce the risk of fire or electric shock, do not
e
xpose this equipment to rain or moisture.
To avoid electrical shock, do not open the
cabin
et. Refer servicing to qualified personnel
only.
No modification of this equipment is allowed.
Warning
To avoid the risk of electric shock, this
equipment must only be connected to a supply
mains with protective earth.
Warning
To disconnect the main power, unplug the power
plug.
When installing the unit, incorporate a readily
a
ccessible disconnect device in the fixed wiring, or
connect the power plug to an easily accessible
socket-outlet near the unit.
Do not position the ME equipment where it is
di
fficult to unplug the power plug.
If a fault should occur during operation of the unit,
op
erate the disconnect device to switch the power
supply off, or disconnect the power plug.
Warning
Symbols on the product
Safety sign
Follow the warnings in the instructions
f
or use for parts of the unit on which this
symbol appears.
NOTE Background color: Blue
Symbol: White
Consult the instructions for use
Follow the directions in the instructions
for use for parts of the unit on which this
symbol appears.
This symbol indicates the manufacturer,
and appears next to the manufacturer’s
n
ame and address.
This symbol indicates the Importer, and
appears next to the Importer’s name and
re
gistered office address.
This symbol indicates the European
Community representative, and appears
n
ext to the European Community
representative’s name and address.
This symbol indicates the UK
Responsible Person, and appears next to
the
UK Responsible Person’s name and
address.
This symbol indicates the Swiss
authorized representative, and appears
ne
xt to the Swiss authorized
representative’s name and address.
This symbol indicates the medical device
in the European Community.
This symbol indicates the date of
manufacture.
This symbol indicates the serial number.
This symbol indicates the Unique Device
Identifier (UDI), and appears next to the
b
ar code representation of the Unique
Device Identification.
This symbol indicates the equipotential
terminal which brings the various parts
o
f a system to the same potential.
Storage and transport temperature
This symbol indicates the acceptable
t
emperature range for storage and
transport environments.
Storage and transport humidity
This symbol indicates the acceptable
humid
ity range for storage and transport
environments.
Storage and transport pressure
This symbol indicates the acceptable
atmosp
heric pressure range for storage
and transport environments.
3
For customers in the U.S.A.
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.
You are cautioned that any changes or
mo
difications not expressly approved in this
manual could void your authority to operate this
equipment.
All interface cables used to connect peripherals
must b
e shielded in order to comply with the
limits for a digital device pursuant to Subpart B of
part 15 of FCC Rules.
If you have any questions about this product, you
may call;
Sony Customer Information Service Center 1-800-
22
2-7669 or http://www.sony.com/
For customers in the U.S.A.
Caution
Federal law (United States of America) restricts
this device to sale by or on the order of a licensed
healthcare practitioner.
For customers in Canada
This unit has been certified according to Standard
CAN/CSA-C22.2 No. 60601-1.
For customers in Europe
Any serious incident that has occurred in relation
to the device should be reported to the
manufacturer and the competent authority of the
Member State in which the user and/or patient is
established.
Supplier’s Declaration of Conformity
Trade Name : SONY
Model : LMD-X2705MD
LMD-X2700MD
Responsible party : Sony Electronics Inc.
Address : 16535 Via Esprillo,
San Diego, CA 92127 U.S.A.
Telephone Number: 858-942-2230
This device complies with part 15 of the FCC
Ru
les. Operation is subject to the following two
conditions: (1) This device may not cause
ha
rmful interference, and (2) this device must
accept any interference received, including
interference that may cause undesired
operation.
Product Specifications
| Brand: | Sony |
| Category: | Monitor |
| Model: | LMD-X2705MD |
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