Sony LMD-X2700MD Bruksanvisning

Sony Følge LMD-X2700MD

Les nedenfor 📖 manual på norsk for Sony LMD-X2700MD (38 sider) i kategorien Følge. Denne guiden var nyttig for 20 personer og ble vurdert med 4.5 stjerner i gjennomsnitt av 2 brukere

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Side 1/38

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

2024-04

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,

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

nvironments, such as doctors’ offices,

examination rooms, and operating rooms.

To reduce the risk of fire or electric shock, do not

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

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

fficult to unplug the power plug.

If a fault should occur during operation of the unit,

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

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

ame and address.

This symbol indicates the Importer, and

appears next to the Importer’s name and

gistered office address.

This symbol indicates the European

Community representative, and appears

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

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

ar code representation of the Unique

Device Identification.

This symbol indicates the equipotential

terminal which brings the various parts

f a system to the same potential.

Storage and transport temperature

This symbol indicates the acceptable

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.

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

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-

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

les. Operation is subject to the following two

conditions: (1) This device may not cause

rmful interference, and (2) this device must

accept any interference received, including

interference that may cause undesired

operation.

Produkspesifikasjoner

Merke:	Sony
Kategori:	Følge
Modell:	LMD-X2700MD

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