Bayer HealthCare Clinitek 500, Руководство по эксплуатации

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1.4
Revised 5/03
Specifications
Power Required:
100–240 VAC 10%, 50–60 Hz
Maximum Power Input:
72 VA
Fuse Rating: (not user-replaceable)
2A, 250 V, 2AG, SB(T)
*Line Leakage Current:
<0.5 milliamperes in normal condition
<3.5 milliamperes in single fault condition
Heat Output:
Approximately 246 BTU/hour
Dimensions:
Depth — 32.4 cm (12.8 in.)
Width — 37.7 cm (14.8 in.)
Height — 28.2 cm (11.1 in.)
Weight:
7.4 kg (16.3 lb.)
Ambient Operating Temperature Range:
18°C to 30°C (64°F to 86°F)
Ambient Operating Humidity Range:
20% to 80% relative humidity
Optimum Operating Conditions:
22°C to 26°C (72°F to 79°F);
35% to 55% relative humidity
NOTE: Because of the nature of the urobilinogen and
leukocyte reagents found on Bayer Reagent Strips,
these two results may be decreased at temperatures
below 22°C (72°F) and increased at temperatures
above 26°C (79°F).
Safety Standards:
The CLINITEK ® 500 Urine Chemistry Analyzer (Model
6470) is listed by the Underwriters’ Laboratories ( )
and the Canadian Standards Association ( ) as cer-
tified and complies with the safety standards specified
in UL 3101 and CSA-C22.2, No. 1010.1. The instru-
ment meets the provisions of the IVD Directive 98/79/EC
(Oct./1998) (
), which includes the EMC Directive
89/336 Amendment 92/31/EEC and the Low Voltage
Safety Directive 73/23/EEC.
The safety standards specify that the instrument must
operate safely in the following conditions:
• indoor use only
• installation category II (IEC 1010)
• pollution degree 2 (IEC 1010)
• maximum altitude 2000 meters (6560 feet)
Warning:
The instrument is for professional, in vitro diagnostic
use ( ) and must be used in the manner specified
in the Operating Manual in order to provide the safety
and performance standards specified.
Symbols on Back of Analyzer:
Centronics Port
(Parallel) for Printer
Serial Port (RJ45)
for Bar Code Reader
Not a telephone jack
Serial Port (RJ45)—
not currently active
Serial Port (EIA-232D)
for host computer
Serial Number
ASTM Software Interface:
Conforms to ASTM E 1381-91, “Specification for Low-
Level Protocol to Transfer Messages between clinical
laboratory instrument and computer systems” and
ASTM E 1394-91, “Specification for Transferring
Information Between Clinical Instruments and Computer
Systems.”
INTRODUCTION
*Testing protocol and allowable limits as specified by the safety
standards for laboratory equipment outlined in UL 3101-1, CSA 22.2
No. 1010.1, and IEC 1010-1.
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