Accelerated Care Plus 1203000C, Руководство пользователя

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OMNISOUND
®
3000C PRO USER MANUAL 27
COPYRIGHT © 2001 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED
TECHNICAL SPECIFICATIONS
GENERAL:
Dimensions:
5" (12.7 cm) H x 9" (22.8 cm) W x 18" (45.7 cm) D
Weight:
25 lbs (11.3 kg)
Operating Power: 120/240VAC; 50/60Hz; 50W
Display System: Super Twist LCD full character display with adjustable contrast /viewing angle.
System Architecture: CMOS integrated micro-controller with on board memory and instruction set.
ULTRASOUND GENERATOR:
Frequency: 1 MHz + 10% or 3 MHz + 10%
Indication Accuracy: + 20% for all levels greater than 1 watt.
Output Display:
Shows total Watts or Watts/cm2 during the Ac/- 20% for all levels greater than 1 watt.
Pulsed Mode:
Output is continuous or pulsed. In pulsed mode output is 100% square wave modulated. Power level is
adjusted with intensity control which controls pulse amplitude.
Continuous Mode: Output is on as long as the timer has time remaining and the output control is turned up.
Delta T Mode:
Output time is calculated based on treatment intensity to achieve a 1, 2, or 4o C temp increase in 2 x ERA
muscle tissue load.
RTPA Duty Factor Pulse Duration Pulse Repetition Rate
+ 20% + 20%
1:1 100% continuous continuous
2:1 50% 2 ms 250Hz
3:1 33% 2 ms 165Hz
4:1 25% 2 ms 125Hz
5:1 20% 2 ms 100Hz
10:1 10% 2 ms 50Hz
20:1 5% 2 ms 25Hz
ULTRASOUND APPLICATOR:
Piezoelectric Disk:
Lead zirconate titanate
Frequency: 1 MHz + 10% or 3 MHz + 10%
ERA/BNR:
Effective Radiating Area (ERA) and Beam Non-Uniformity Ratio (BNR):
1MHz 2cm2 1MHz 5cm2
ERA 1.75 + 60% 5.0 + 50%
BNR < 5:1 < 5:1
Nominal 2.5:1 3.0:1
3MHz 2cm2 3MHz 5cm2
ERA 1.75 + 60% 5.0 + 50%
BNR < 5:1 < 5:1
Nominal 2.5:1 3.0:1
PATIENT SAFETY SYSTEMS:
Activation:
Patient safety hand control shuts down output. Output modality may not be changed during operation.
Output levels are reset to zero at the start and completion of treatment.
MISC:
Treatment Programs:
Output intensity is gradually increased during treatment from 0 to 20% automatically in a linear manner over
the duration of the treatment when the anti-adaptation mode is selected. The amount of the increase is user
programmable.
Certificates and Approvals:
Devices are designed to meet or exceed all safety requirements of a medical device in its class per IEC
60601 and CSA C22.2 No. 601.1
Caution:
Federal law restricts this device to sale by or on the order of a physician (or other health practitioner
licensed by their State).
ACP reserves the right to change technical specifications and product availability without notice.