Elo TouchSystems 1528L Manual do Utilizador descarregar pdf (Página 2)

1528L 15" LCD Medical Touchmonitor

North America

TE Touch Solutions

301 Constitution Drive

Menlo Park, CA 94025-1110

Europe

Tel +32 (0)16 35 21 00

Fax +32 (0)16 35 21 01

[email protected]

800-ELO-TOUCH

Tel 1-650-361-4800

Fax 1-650-361-4722

eloinfo@elotouch.com

Asia-Pacific

Tel +81 (45) 478-2161

Fax +81 (45) 478-2180

www.tps.co.jp

Latin America

Tel 786-923-0251

Fax 305-931-0124

www.elotouch.com.ar

To find out more about our extensive range of Elo touch solutions, go to www.elotouch.com, or call the office nearest you.

Tyco Electronics Corporation and its Affiliates in the TE Touch Solutions business unit of the TE Connectivity Ltd.

family of companies (collectively “TE”) reserves the right to change or update, without notice, any information

contained herein; to change, without notice, the design, construction, materials, processing or specifications of

any products; and to discontinue or limit production or distribution of any products.

AccuTouch, Elo (logo), Elo TouchSystems, IntelliTouch, TE Connectivity, TE connectivity (logo) and TE (logo)

are trademarks of the TE Connectivity Ltd. family of companies.

Case/Bezel Color Dark gray or beige

Base Tall

Display Size: 15" diagonal

Type: Active matrix TFT LCD

Aspect ratio: 4 x 3

Useful Screen Area Horizontal: 11.98" (304 mm); Vertical: 8.98" (228 mm)

Monitor Dimensions Width: 13.99" (355 mm); Height (inc. base): 13.8” (350 mm); Depth (inc. base): 8” (203 mm)

(max, with tall stand)

Optimal (Native) Resolution 1024 x 768

Other Supported Resolutions 1024 x 768 at 60, 65, 70 or 75 Hz; 832 x 624 at 75 Hz; 800 x 600 at 56, 60, 72 or 75 Hz;

720 x 400 at 70 Hz; 720 x 350 at 70 Hz; 640 x 480 at 60, 66 Hz (Mac), 72 or 75 Hz

Colors 16.2 million colors, 8 bit with dithering

Brightness (typical) LCD panel: 350 nits; with AccuTouch: 287 nits; with IntelliTouch: 322 nits

Response Time (typical) 8 ms

Viewing Angle Horizontal (left/right): ±75° or 150° total

(typical, from center) Vertical (up/down): 75°/50° or 125° total

Contrast Ratio 400:1

Input Video Format RGB analog; DVI-D

Input Video Signal Connector Mini D-Sub 15-Pin VGA type; DVI-D connector

Input Frequency Horizontal: 31-60 kHz; Vertical: 56-75 Hz

Power Supply Type: External Power Adapter; DC output (line) voltage: 12.0V ± 0.75V; AC input (line)

voltage to DC adaptor: 100-240 VAC, 50/60 Hz; Power: 48 W max; Hospital grade power

cord for US/CAN; European power cord

Temperature Operating: 0°C to 40°C; Storage: -20°C to 60°C

Humidity Operating: 20-80%; Storage: 5-95% non-condensing

Weight Weight with power adapter: 16.13 lbs (8.3 kg)

(approx., with all options) Weight w/o power adapter: 15.3lbs (6.9 kg)

Shipping Weight: 22.2 lbs ( 10.1 kg)

Warranty Monitor: 3 years

Backlight lamp life Minimum 40,000 hours to half brightness

MTBF 50,000 hours demonstrated

Agency Approvals FCC/IC/C-Tick Class B, UL/cUL Medical UL 60601-1(formerly 2601-1)/C22.2 No. 601.1, CE

Includes EMC requirements EN/IEC 60601-1-2.

Speakers Two-watt/channel speakers located in display head

On-screen Display (OSD) OSD lockouts for power and user controls

User's Controls OSD control menu: menu, up, down, select, power; OSD controls: contrast, brightness,

V-position, H-position, RGB, volume, Sharpness, phase, clock, OSD H-position, OSD

V-position, OSD time, auto adjust, OSD language (English, French, German, Spanish,

Japanese), input select; OSD disable/enable: power, OSD menu

Mounting Options 75 mm VESA mount; Removable base

MEDICAL AND HEALTHCARE APPLICATION DISCLAIMER: It is the sole responsibility of any person intending to commercialize, market or

use any of TE Connectivity Ltd. or its family of companies (“TE”) products for medical or healthcare applications to ensure that such

product is adequate and appropriate for the person’s intended use and complies with all applicable laws, regulations, codes and standards

including but not limited to the European Union Medical Device Directive, United States Federal Food, Drug, and Cosmetic Act, regulations

of the United States Food and Drug Administration (FDA), and for obtaining and maintaining any required regulatory approvals including

but not limited to any required market clearances. TE has not sought nor received any rulings from the FDA or any other federal, state, or

local government agency or notified body as to the safety, effectiveness or appropriateness of its product for such applications. Persons

intending to evaluate or use TE’s product for medical or healthcare purposes must rely on their own medical and legal judgment without

any representation on the part of TE.

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