Technical Specifications - Accelerated Care Plus OMNISOUND 3000C PRO User Manual

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OMNISOUND 3000C PRO USER MANUAL
GENERAL:
Dimensions:
Weight:
Operating Power:
Display System:
System Architecture:
ULTRASOUND GENERATOR:
Frequency:
Indication Accuracy:
Output Display:
Pulsed Mode:
Continuous Mode:
Delta T Mode:
RTPA
1:1
2:1
3:1
4:1
5:1
10:1
20:1
ULTRASOUND APPLICATOR:
Piezoelectric Disk:
Frequency:
ERA/BNR:
PATIENT SAFETY SYSTEMS:
Activation:
MISC:
Treatment Programs:
Certificates and Approvals:
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.
COPYRIGHT © 2001 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED

TECHNICAL SPECIFICATIONS

5" (12.7 cm) H x 9" (22.8 cm) W x 18" (45.7 cm) D
25 lbs (11.3 kg)
120/240VAC; 50/60Hz; 50W
Super Twist LCD full character display with adjustable contrast /viewing angle.
CMOS integrated micro-controller with on board memory and instruction set.
1 MHz + 10% or 3 MHz + 10%
+ 20% for all levels greater than 1 watt.
Shows total Watts or Watts/cm 2 during the Accuracy +/- 20% for all levels greater than 1 watt.
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.
Output is on as long as the timer has time remaining and the output control is turned up.
Output time is calculated based on treatment intensity to achieve a 1, 2, or 4 o C temp increase in 2 x ERA
muscle tissue load.
Duty Factor
+ 20%
100%
50%
33%
25%
20%
10%
5%
Lead zirconate titanate
1 MHz + 10% or 3 MHz + 10%
Effective Radiating Area (ERA) and Beam Non-Uniformity Ratio (BNR):
1MHz 2cm 2
ERA 1.75 + 60%
BNR < 5:1
Nominal 2.5:1
3MHz 2cm 2
ERA 1.75 + 60%
BNR < 5:1
Nominal 2.5:1
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.
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.
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
Pulse Duration
+ 20%
continuous
2 ms
2 ms
2 ms
2 ms
2 ms
2 ms
1MHz 5cm 2
5.0 + 50%
< 5:1
3.0:1
3MHz 5cm 2
5.0 + 50%
< 5:1
3.0:1
27
Pulse Repetition Rate
continuous
250Hz
165Hz
125Hz
100Hz
50Hz
25Hz