Instrukcja obsługi Sony LMD-X310MT
Przeczytaj poniżej 📖 instrukcję obsługi w języku polskim dla Sony LMD-X310MT (45 stron) w kategorii monitor. Ta instrukcja była pomocna dla 18 osób i została oceniona przez 2 użytkowników na średnio 4.5 gwiazdek
Strona 1/45
4-596-096-16(1)
LCD Monitor
Instructions for Use
Before operating the unit, please read this manual thoroughly
and retain it for future reference.
LMD-X310MT
LMD-X550MT
© 2016 Sony Corporation
2021-09
2
Indications for Use/Intended Use
The LCD Monitor is intended to provide 4K, 3D and 2D
color video displays of images from endoscopic/
laparoscopic camera systems, surgical microscope and
other compatible medical imaging systems.
The LCD Monitor is a widescreen, high-definition,
medical 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
environments, such as clinics, examination rooms, and
operating rooms.
• Essential performance is to display image and operate
functions normally.
To reduce the risk of fire or electric shock, do not
expose this equipment to rain or moisture.
To avoid electrical shock, do not open the
cabinet. Refer servicing to qualified personnel
only.
No modification of this equipment is allowed.
WARNING
Symbols on the product
Safety sign (LMD-X310MT only)
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 name and
address.
This symbol indicates the EU Importer, and
appears next to the EU Importer’s name and
address.
This symbol indicates the European
Community representative, and appears next
to the European Community 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 version of the
accompanying document.
This symbol indicates the Unique Device
Identifier (UDI), and appears next to the bar
code representation of the Unique Device
Identification.
This symbol indicates the equipotential
terminal which brings the various parts of a
system to the same potential.
Storage and transport temperature
This symbol indicates the acceptable
temperature range for storage and transport
environments.
Storage and transport humidity
This symbol indicates the acceptable humidity
range for storage and transport environments.
Storage and transport pressure
This symbol indicates the acceptable
atmospheric pressure range for storage and
transport environments.
Parts on the unit with this symbol have a risk
of electric shock. Follow the cautions in the
instructions for use.
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 modifications not
expressly approved in this manual could void your
authority to operate this equipment.
All interface cables used to connect peripherals must be
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
This unit has been certified according to Standard CAN/
CSA-C22.2 No. 60601-1.
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, IEC 60950-1,
and IEC 60065 standards and other IEC/ISO
standards applicable to the devices.
2. Furthermore, the system as a whole must comply with
IEC 60601-1 standards. All peripheral 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 increase the
leakage current.
4. For all peripheral devices connected to the unit that
operate on commercial power supplies and do not
comply with IEC 60601-1 standards, incorporate an
isolation transformer that complies with IEC 60601-1
standards and connect to the commercial power
supply via the transformer.
5. The unit generates, uses, and may radiate radio
frequency 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
devices.
– Connect the unit and the affected devices to
different branch circuits.
For more information, consult qualified Sony service
personnel.
(Applicable standard: IEC 60601-1-2)
Specyfikacje produktu
| Marka: | Sony |
| Kategoria: | monitor |
| Model: | LMD-X310MT |
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