26
Technical specifications
System power supply
Voltage
100–240 VAC
Frequency
50–60 Hz
Connected load
≤
2.2 Amps
Fuses
Type
T3.15A L 250V
Quantity
2
Classification
Protection class
Class I (with protective earth [=ground])
IPX0, continuous operation
Type
BF (with hand-held FG, targeting probe)
Humidity
No protection
Explosion
No protection
Ambient conditions
Temperature
10–40°C
Humidity
30–75% RH (non-condensing)
Air pressure
700–1060 HPa
Storage and transport
Temperature
-20–50°C
(in original packaging)
Humidity
10–90% RH (non-condensing)
Air pressure
700–1060 HPa
System
Dimensions (DxWxH)
40cm x 38cm x 20cm
Weight
9kg
Transportation case
Dimensions (DxWxH)
63cm x 50cm x 35cm
case + accessories Weight
≈
20kg
Complies with standards
USA, Canada, Europe
IEC 60601-1 (2nd edition)
IEC 60601-1-2:2007
CSA C22.2#601-1 (2nd edition)
Electrical safety
The system meets IEC standards (eg IEC 60601). All configurations comply with standard
IEC 60601-1-1. Any person connecting equipment to the system is responsible for the configuration
and must ensure that it complies with system standard 60601-1-1 or equivalent national standards.
Please contact your customer service representative in the event of any queries.
Note The system may reboot after a power line surge greater than 1KV. This is considered a normal
condition and the system will automatically reboot to the software application.
Note Only use 110V/60Hz AC connection when powering the Trauma Interface within the United
States. The Trauma Interface is not certified for 220V/60Hz operation within the United States.
Note This equipment is not suitable for use in the presence of a flammable anesthetic mixture with
air, oxygen, or nitrous oxide.
Note To ensure proper operation, no other electrical components should be located near the
TRIGEN™ SURESHOT™ Distal Targeting unit.
Smith & Nephew reserves the right to make any technical changes.
Содержание TRIGEN SURESHOT
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