Sony LMD-2435MD Manual
Read below đź“– the manual in Italian for Sony LMD-2435MD (37 pages) in the Monitor category. This guide has been helpful for 32 people and has been rated 4.5 stars on average by 2 users
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4-584-947-17(1)
LCD Monitor
Instructions for Use
Before operating the unit, please read this manual thoroughly
and retain it for future reference.
LMD-2735MD
LMD-2435MD
© 2016 Sony Corporation
2024-04
2
Indications for Use/Intended Use
The Sony LMD-2735MD/2435MD LCD Monitor are
intended to provide 2D color video displays of
images from surgical endoscopic/laparoscopic
camera systems and other compatible medical
imaging systems.
The LMD-2735MD/2435MD monitor are a
w
idescreen, high-definition, medical grade
monitor for real-time use during minimally
invasive surgical procedures and are 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.
Essential performance is to display image and
o
perate functions normally.
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
This unit has no power switch.
To disconnect the main power, unplug the power
pl
ug.
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
for 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.
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.
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
CAN ICES-3 (A)/NMB-3(A)
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.
Important safeguards and notices for use
in the medical environments
1. All devices connected to the unit must be
certified or compliant according to IEC 60601-1,
IE
C 60950-1, IEC 62368-1 and IEC 60065
sta
ndards and other IEC/ISO standards
applicable to the devices.
2. Furthermore, the system as a whole must
comp
ly with IEC 60601-1 standards. All
p
eripheral devices connected to the signal
input/output sections of the unit constitute the
medical-use system, and therefore, the user is
responsible for ensuring that the system as a
whole complies with IEC 60601-1 standards. If
in
doubt, consult qualified Sony service
personnel.
3. Connecting the unit to other devices may
in
crease the leakage current.
4. For all peripheral devices connected to the unit
th
at operate on commercial power supplies
and do not comply with IEC 60601-1 standards,
in
corporate an isolation transformer that
complies with IEC 60601-1 standards and
conn
ect to the commercial power supply via
the transformer.
5. The unit generates, uses, and may radiate radio
fr
equency energy. If it is not installed and used
in accordance with the instruction manual, it
may cause interference on other devices. If the
unit causes interference (which can be
determined by disconnecting the power cord
from the unit), try the following.
– Relocate the unit with respect to the affected
de
vices.
– Connect the unit and the affected devices to
dif
ferent branch circuits.
For more information, consult qualified Sony
serv
ice personnel.
(Applicable standard: IEC 60601-1-2)
Storage and transport humidity
This symbol indicates the acceptable
h
umidity range for storage and transport
environments.
Storage and transport pressure
This symbol indicates the acceptable
atmo
spheric pressure range for storage
and transport environments.
Product Specifications
| Brand: | Sony |
| Category: | Monitor |
| Model: | LMD-2435MD |
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