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Home  >  Electrotherapy  >  Russian Stimulator  >  Roscoe Medical Combo Care - An E-Stim and Ultrasound Combo Professional Device
UPC: 092237605462
Code: koalaty-60546

Roscoe Medical Combo Care - An E-Stim and Ultrasound Combo Professional Device

Roscoe Medical Combo Care - An E-Stim and Ultrasound Combo Professional Device
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Retail Price: $1,799.95
Your price: $999.95
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  • Description
  • Features
  • Warnings
  • Includes
  • Technical
  • Warranty
  • More
Current Solutions™ ComboCare™ E-Stim and Ultrasound Combo Professional Device - 1 ea.
All-In-One E-Stim and Ultrasound Combo Professional Device with therapeutic ultrasound and 5 waveforms: IF 4- and 2-Pole, Russian, TENS, and EMS.

The Combo Care™ E-Stim and Ultrasound Combo Professional Device is a professional dual channel ultrasound and electrotherapy device. It contains 5 electrotherapy waveforms that include: Interferential 4-Pole, Interferential 2-Pole, Russian, EMS, and TENS. It also has 10 preset programs for each of the five electrotherapy waveforms and 10 Ultrasound preset programs making a total of 60 preset programs to use. The design makes it easy to use on a tabletop, therapy cart, or for mobile use. It also has a large and easy to read LCD display, exact dial performance, and a programmable timer. The advanced technological operating system ensures a complete range of therapy no matter where you use it.

  • All-In-One E-Stim and Ultrasound Combo Professional Device
  • Waveforms:
    • Interferential (4-Pole)
    • Premodulated (2-Pole Interferential)
    • Medium Frequency (Russian)
    • Electronic Muscle Stimulation
    • Transcutaneous Electrical Nerve Stimulation
  • Therapeutic Ultrasound
  • 10 Presets Per Waveform
  • 20 Ultrasound Presets
  • Large Easy-To-Read Graphic LCD Display
  • Exact Dial Performance
  • Programmable Timer
  • Designed for tabletop, therapy cart, or mobile use

Questions: Call Manufacturer at 1-800-871-7858 or Visit: www.roscoemedical.com

Features:

  • Dual Channel
  • Five Waveforms
  • 10 Presets Per Waveform
  • 20 Ultrasound Presets
  • Large Easy-To-Read Graphic LCD Display
  • Exact Dial Performance
  • Programmable Timer
  • Designed for tabletop, therapy cart, or mobile use

General Technical Specifications:

  • Dimensions: 9.8" (W) x 7.3 (L) x 3.2 (H)
  • Adapter Supply Voltage: 100-240 V, 47-63 Hz, 1.35A
  • Adapter Output: 15V 3A Max.
  • Adapter Dimensions: 143mm (L) x 73mm (W) x 40mm (H)
  • Dimensions: 250mm (L) x 185mm (W) x 82 mm (H)
  • Operating Environment:
    • Temperature: 10°C (50°F) to 40°C (104°F)
    • Relative Humidity: 30% - 85%
  • Storage Environment:
    • Temperature: -20°C (-4°F) to 55°C (131°F)
    • Relative Humidity: 20% - 90%
  • Maximum Treatment Time: 60 minutes - electrical stimulation

Technical Specifications:

  • Ultrasonic Generator Mode
    • Frequency: 1MHz ± 10%, 3MHz ± 10%
    • Duty Factor: 10% - 100%, Stepping 10%
    • Pulse Repetition Rate: 100 Hz
    • Treatment Time: Max. 30 minutes
    • Output Power:
      • 0.5 - 10 W, when duty factor > 80% for 5cm²
      • 0.5 - 15 W, when duty factor < 70% for 5cm²
      • 0.1 - 2 W, when duty factor > 80% for 1cm²
      • 0.1 - 3 W, when duty factor < 70% for 1cm²
    • Effective Radiating Area (AER): 1 cm² (Optional) 5 cm²
    • Effective Intensity (Max): 3 W/cm²
    • Indication Accuracy: ± 20% (for any level above 10% of Maximum)
    • RBN (Max): < 8.0
    • Beam Type: Collimated
    • Material of Sound Head: Aluminum
  • 4-Pole Interferential Mode:
    • Waveform Type: Bi-aphasic square
    • Mode Selection: CC (Constant Current) or CV (Constant Voltage)
    • Vector: Auto: 0%-100%; Manual: 0%-90%
    • Carrier Frequency (CF): 4.0kHz
    • Sweep Low Beat Frequency (Beat H.): (Beat L.) - 150 Hz
    • Sweep High Beat Frequency (Beat L.): 1 - (Heat H.) Hz
    • Output Intensity: 0-100 mA (CC at 1k ohm load); 0-100V (CV at 1k ohm load)
    • Treatment Time: 1-60 minutes
  • 2-Pole Interferential Mode:
    • Waveform Type: Bi-phasic square
    • Mode Selection: CC (Constant Current) or CV (Constant Voltage)
    • Carrier Frequency: 2.5 kHz
    • Sweep Low Beat Frequency (Beat H.): (Beat L.) - 150 Hz
    • Sweep High Beat Frequency (Beat L.): 1 - (Heat H.) Hz
    • Output Intensity: 0-100 mA (CC at 1k ohm load); 0-100V (CV at 1k ohm load)
    • Treatment Time:1-60 minutes
    • Cycle Time (Cycle): Continuous, 5/5, 4/12, 10/10, 10/20, 10/30, 10/50
    • Ramp Time (Ramp): 2 seconds
  • TENS and EMS Mode:
    • Waveform Type: Mono- or Bi-phasic square
    • Mode Selection: CC (Constant Current) or CV (Constant Voltage)
    • Frequency: 1-250 Hz
    • Frequency Modulation (FM): 0-249 Hz
    • Burst Rate (Burst): 0-10 Hz (7 pulse)
    • Phase Duration (P.Dur): 30-400 µs
    • Amplitude Modulation (AM): 0% - 100%
    • Output Intensity: 0-100 mA (CC at 1k ohm load); 0-100V (CV at 1k ohm load)
    • Cycle Time (Cycle): Continuous, 4/4, 4/8, 7/7, 5/5, 4/12, 10/10, 10/20, 10/30, 10/50
    • Treatment Time: 1-60 minutes
    • Ramp Time: 1 second
  • Russian Mode:
    • Waveform Type: Bi-phasic square
    • Mode Selection: CC (Constant Current) or CV (Constant Voltage)
    • Carrier Frequency (CF): 2.5 kHz
    • Burst Frequency (Freq.): 20-100 Hz
    • Output Intensity: 0-100 mA (CC at 1k ohm load); 0-100V (CV at 1k ohm load)
    • Duty Cycle: 10%, 20%, 30%, 40%, and 50%
    • Treatment Time: 1-60 minutes
    • Ramp Time (Ramp): 1s, 2s, and 5s

Package Includes:

  • 2 Rubber Electrodes (60 x 90mm)
  • 2 Rubber Electrodes (70 x 110mm)
  • 2 Electrode Sponges (70 x 110mm)
  • 2 Electrode Sponges (80 x 120mm)
  • 4 (50 x 50mm) adhesive electrodes
  • 4 (50 x 100mm) adhesive electrodes
  • Elastic Wrap (75 x 1200mm)
  • Elastic Wrap (75 x 600mm)
  • 2 Electrode Wires (black/red)
  • Adapter (100-250 V) (47-63 Hz)
  • Power Cord
  • Electrical Stimulation Cable
  • Electrode Wire for Ultrasound Combination
  • 5 cm² Aer Ultrasound Applicator
  • Operating Manual

Warnings:

  • USA Federal Law restricts these devices to sale by, or on the order of, a physician or licensed practitioner. This device should be used only under the continued supervision of a physician or licensed practitioner.
  • Make certain the unit is electrically grounded by connecting only to a grounded electrical service receptacle conforming to the applicable national and local electrical codes.
  • Care must be taken when operating this equipment around other equipment. Potential electromagnetic or other interference could occur to this or to the other equipment. Try to minimize this interference by not using other equipment in conjunction with it.
  • Before administering any treatment to a patient you should become acquainted with the operating procedures for each mode of treatment available, as well as the indications, contradictions, warnings and precautions. Consult other resources for additional information regarding the application of electrotherapy and Ultrasound.
  • To prevent electrical shock, disconnect the unit from the power source before attempting any maintenance procedures.
  • The use of accessories, transducers and cables than those specified, with the exception of transducers and cables sold by the manufacturer as replacement parts for internal components, may result in increased emissions or decreased  immunity of the device.
  • This device is not designed to be use in an MRI Environment and should be removed prior to MRI exposure.
  • Do not apply stimulation over the patient's neck because this could cause severe muscle spasms resulting in closure of the airway, difficulty in breathing, or adverse effects on heart rhythm or blood pressure;
  • Do not apply stimulation across the patient's chest, because the introduction of electrical current into the chest may cause rhythm disturbances to the patient's heart, which could be lethal;
  • Do not apply stimulation over open wounds or rashes, or over swollen, red, infected, or inflamed areas or skin eruptions (e.g., phlebitis, thrombophlebitis, varicose veins);
  • Do not apply stimulation over, or in proximity to, cancerous lesions;
  • Do not apply stimulation in the presence of electronic monitoring equipment (e.g., cardiac monitors, ECG alarms), which may not operate properly when the electrical stimulation device is in use;
  • Do not apply stimulation when the patient is in the bath or shower;
  • Do not apply stimulation while the patient is sleeping; and
  • Do not apply stimulation while the patient is driving, operating machinery, or during any activity in which electrical stimulation can put the patient at risk of injury.
  • Consult with the patient's physician before using this device, because the device may cause lethal rhythm disturbances to the heart in susceptible individuals; and
  • Apply stimulation only to normal, intact, clean, healthy skin.
  • This device should not be used for symptomatic local pain relief unless etiology is established or unless a pain syndrome has been diagnosed. Patients with arterial or venous thrombosis or thrombophlebitis are at risk of developing embolisms when electrical stimulation is applied over or adjacent to the vessels containing the thrombus. If a patient has a history of deep vein thrombosis, even many years past, the affected area should not be stimulated.
  • Fresh fractures should not be stimulated in order to avoid unwanted motion.
  • Stimulation should not be applied immediately following trauma or to tissues susceptible to hemorrhage.
  • Do not apply electrodes directly over the eyes or inside body cavities.
  • Do not use electrical stimulation in conjunction with high frequency surgical equipment or microwave or shortwave therapy systems.
  • Keep electrodes separated during treatment. Electrodes in contact with each other could result in improper stimulation or skin burns.
  • Since the effects of stimulation of the brain are unknown, stimulation should not be applied across the head, and electrodes should not be placed on opposite sides of the head.

Warranty:

  • The following warranty terms apply:
    • The warranty period for ComboCare™ products is 2 years from date of purchase.
    • Defects in material or workmanship will be removed free of charge with in the warranty period.
    • Repairs under warranty do not extend over the warranty period either for the device or the replacement parts.
  • The following is excluded under the warranty:
    • All damage which has arisen due to improper treatment, e.g. nonobservance of the user instruction.
    • All damage which is due to repairs or tampering by the customer or unauthorized third parties.
    • Damage which has arisen during transport from the manufacturer to the consumer or during transport to the service center.
    • Accessories which are subject to normal wear and tear.
    • Liability for direct or indirect consequential losses caused by the unit is excluded even if the damage to the unit is accepted as a warranty claim.

Current Solutions
3814 Woodbury Drive
Austin, TX, 78704
©www.roscoemedical.com

Product Reviews

Features:

  • Dual Channel
  • Five Waveforms
  • 10 Presets Per Waveform
  • 20 Ultrasound Presets
  • Large Easy-To-Read Graphic LCD Display
  • Exact Dial Performance
  • Programmable Timer
  • Designed for tabletop, therapy cart, or mobile use

Warnings:

  • USA Federal Law restricts these devices to sale by, or on the order of, a physician or licensed practitioner. This device should be used only under the continued supervision of a physician or licensed practitioner.
  • Make certain the unit is electrically grounded by connecting only to a grounded electrical service receptacle conforming to the applicable national and local electrical codes.
  • Care must be taken when operating this equipment around other equipment. Potential electromagnetic or other interference could occur to this or to the other equipment. Try to minimize this interference by not using other equipment in conjunction with it.
  • Before administering any treatment to a patient you should become acquainted with the operating procedures for each mode of treatment available, as well as the indications, contradictions, warnings and precautions. Consult other resources for additional information regarding the application of electrotherapy and Ultrasound.
  • To prevent electrical shock, disconnect the unit from the power source before attempting any maintenance procedures.
  • The use of accessories, transducers and cables than those specified, with the exception of transducers and cables sold by the manufacturer as replacement parts for internal components, may result in increased emissions or decreased  immunity of the device.
  • This device is not designed to be use in an MRI Environment and should be removed prior to MRI exposure.
  • Do not apply stimulation over the patient's neck because this could cause severe muscle spasms resulting in closure of the airway, difficulty in breathing, or adverse effects on heart rhythm or blood pressure;
  • Do not apply stimulation across the patient's chest, because the introduction of electrical current into the chest may cause rhythm disturbances to the patient's heart, which could be lethal;
  • Do not apply stimulation over open wounds or rashes, or over swollen, red, infected, or inflamed areas or skin eruptions (e.g., phlebitis, thrombophlebitis, varicose veins);
  • Do not apply stimulation over, or in proximity to, cancerous lesions;
  • Do not apply stimulation in the presence of electronic monitoring equipment (e.g., cardiac monitors, ECG alarms), which may not operate properly when the electrical stimulation device is in use;
  • Do not apply stimulation when the patient is in the bath or shower;
  • Do not apply stimulation while the patient is sleeping; and
  • Do not apply stimulation while the patient is driving, operating machinery, or during any activity in which electrical stimulation can put the patient at risk of injury.
  • Consult with the patient's physician before using this device, because the device may cause lethal rhythm disturbances to the heart in susceptible individuals; and
  • Apply stimulation only to normal, intact, clean, healthy skin.
  • This device should not be used for symptomatic local pain relief unless etiology is established or unless a pain syndrome has been diagnosed. Patients with arterial or venous thrombosis or thrombophlebitis are at risk of developing embolisms when electrical stimulation is applied over or adjacent to the vessels containing the thrombus. If a patient has a history of deep vein thrombosis, even many years past, the affected area should not be stimulated.
  • Fresh fractures should not be stimulated in order to avoid unwanted motion.
  • Stimulation should not be applied immediately following trauma or to tissues susceptible to hemorrhage.
  • Do not apply electrodes directly over the eyes or inside body cavities.
  • Do not use electrical stimulation in conjunction with high frequency surgical equipment or microwave or shortwave therapy systems.
  • Keep electrodes separated during treatment. Electrodes in contact with each other could result in improper stimulation or skin burns.
  • Since the effects of stimulation of the brain are unknown, stimulation should not be applied across the head, and electrodes should not be placed on opposite sides of the head.

Package Includes:

  • 2 Rubber Electrodes (60 x 90mm)
  • 2 Rubber Electrodes (70 x 110mm)
  • 2 Electrode Sponges (70 x 110mm)
  • 2 Electrode Sponges (80 x 120mm)
  • 4 (50 x 50mm) adhesive electrodes
  • 4 (50 x 100mm) adhesive electrodes
  • Elastic Wrap (75 x 1200mm)
  • Elastic Wrap (75 x 600mm)
  • 2 Electrode Wires (black/red)
  • Adapter (100-250 V) (47-63 Hz)
  • Power Cord
  • Electrical Stimulation Cable
  • Electrode Wire for Ultrasound Combination
  • 5 cm² Aer Ultrasound Applicator
  • Operating Manual

General Technical Specifications:

  • Dimensions: 9.8" (W) x 7.3 (L) x 3.2 (H)
  • Adapter Supply Voltage: 100-240 V, 47-63 Hz, 1.35A
  • Adapter Output: 15V 3A Max.
  • Adapter Dimensions: 143mm (L) x 73mm (W) x 40mm (H)
  • Dimensions: 250mm (L) x 185mm (W) x 82 mm (H)
  • Operating Environment:
    • Temperature: 10°C (50°F) to 40°C (104°F)
    • Relative Humidity: 30% - 85%
  • Storage Environment:
    • Temperature: -20°C (-4°F) to 55°C (131°F)
    • Relative Humidity: 20% - 90%
  • Maximum Treatment Time: 60 minutes - electrical stimulation

Technical Specifications:

  • Ultrasonic Generator Mode
    • Frequency: 1MHz ± 10%, 3MHz ± 10%
    • Duty Factor: 10% - 100%, Stepping 10%
    • Pulse Repetition Rate: 100 Hz
    • Treatment Time: Max. 30 minutes
    • Output Power:
      • 0.5 - 10 W, when duty factor > 80% for 5cm²
      • 0.5 - 15 W, when duty factor < 70% for 5cm²
      • 0.1 - 2 W, when duty factor > 80% for 1cm²
      • 0.1 - 3 W, when duty factor < 70% for 1cm²
    • Effective Radiating Area (AER): 1 cm² (Optional) 5 cm²
    • Effective Intensity (Max): 3 W/cm²
    • Indication Accuracy: ± 20% (for any level above 10% of Maximum)
    • RBN (Max): < 8.0
    • Beam Type: Collimated
    • Material of Sound Head: Aluminum
  • 4-Pole Interferential Mode:
    • Waveform Type: Bi-aphasic square
    • Mode Selection: CC (Constant Current) or CV (Constant Voltage)
    • Vector: Auto: 0%-100%; Manual: 0%-90%
    • Carrier Frequency (CF): 4.0kHz
    • Sweep Low Beat Frequency (Beat H.): (Beat L.) - 150 Hz
    • Sweep High Beat Frequency (Beat L.): 1 - (Heat H.) Hz
    • Output Intensity: 0-100 mA (CC at 1k ohm load); 0-100V (CV at 1k ohm load)
    • Treatment Time: 1-60 minutes
  • 2-Pole Interferential Mode:
    • Waveform Type: Bi-phasic square
    • Mode Selection: CC (Constant Current) or CV (Constant Voltage)
    • Carrier Frequency: 2.5 kHz
    • Sweep Low Beat Frequency (Beat H.): (Beat L.) - 150 Hz
    • Sweep High Beat Frequency (Beat L.): 1 - (Heat H.) Hz
    • Output Intensity: 0-100 mA (CC at 1k ohm load); 0-100V (CV at 1k ohm load)
    • Treatment Time:1-60 minutes
    • Cycle Time (Cycle): Continuous, 5/5, 4/12, 10/10, 10/20, 10/30, 10/50
    • Ramp Time (Ramp): 2 seconds
  • TENS and EMS Mode:
    • Waveform Type: Mono- or Bi-phasic square
    • Mode Selection: CC (Constant Current) or CV (Constant Voltage)
    • Frequency: 1-250 Hz
    • Frequency Modulation (FM): 0-249 Hz
    • Burst Rate (Burst): 0-10 Hz (7 pulse)
    • Phase Duration (P.Dur): 30-400 µs
    • Amplitude Modulation (AM): 0% - 100%
    • Output Intensity: 0-100 mA (CC at 1k ohm load); 0-100V (CV at 1k ohm load)
    • Cycle Time (Cycle): Continuous, 4/4, 4/8, 7/7, 5/5, 4/12, 10/10, 10/20, 10/30, 10/50
    • Treatment Time: 1-60 minutes
    • Ramp Time: 1 second
  • Russian Mode:
    • Waveform Type: Bi-phasic square
    • Mode Selection: CC (Constant Current) or CV (Constant Voltage)
    • Carrier Frequency (CF): 2.5 kHz
    • Burst Frequency (Freq.): 20-100 Hz
    • Output Intensity: 0-100 mA (CC at 1k ohm load); 0-100V (CV at 1k ohm load)
    • Duty Cycle: 10%, 20%, 30%, 40%, and 50%
    • Treatment Time: 1-60 minutes
    • Ramp Time (Ramp): 1s, 2s, and 5s

Warranty:

  • The following warranty terms apply:
    • The warranty period for ComboCare™ products is 2 years from date of purchase.
    • Defects in material or workmanship will be removed free of charge with in the warranty period.
    • Repairs under warranty do not extend over the warranty period either for the device or the replacement parts.
  • The following is excluded under the warranty:
    • All damage which has arisen due to improper treatment, e.g. nonobservance of the user instruction.
    • All damage which is due to repairs or tampering by the customer or unauthorized third parties.
    • Damage which has arisen during transport from the manufacturer to the consumer or during transport to the service center.
    • Accessories which are subject to normal wear and tear.
    • Liability for direct or indirect consequential losses caused by the unit is excluded even if the damage to the unit is accepted as a warranty claim.
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Transcutaneous Electrical Nerve Stimulation (TENS)

TENS is a non-invasive, drug free method of controlling pain, which uses tiny electrical impulses sent through the skin to nerves in order to modify your pain perception. In most people it is effective in reducing or eliminating the pain.

Electronic Muscle Stimulation (EMS)

EMS works by sending electronic pulses to the muscle(s). This is achieved by sending low frequency electric pulses through muscle tissue causing them to gently contract. In this way the muscles are passively exercised and blood flow is increased

Galvanic Stimulators

Galvanic Stimulators use direct current, which creates an electrical field over the treated area. The positive pad works like ice, causing reduced circulation to the area under the pad. The negative pad works like heat, causing increased circulation.

Interferential

IF sends small comfortable electrical impulses through your skin to work on deeper tissue stimulation. The sensation works to prevent pain signals from reaching the brain.

Infrared

Infrared Light Therapy help the body by delivering specific light waveforms that increase circulation. Increasing circulation helps promote healing, lessen swelling, and helps in reducing pain.

Ultrasound

Portable Ultrasounds give advanced pain relief using sonic stimulation of soft tissue cells. They generate pulsed, high frequency sound waves, which travel deep into the tissue, generating vasodilation. This helps increase blood flow to the treated area.

Russian

Russian stimulation uses medium frequencies to provide stimulation to muscle groups. This is used to reduce muscle spasms as well as for muscle strengthening. This method was created to produce maximal muscle strengthening effects.

Micro Current

Microcurrent Therapy uses extremely small amounts of electrical current (millionths of an amp) to help relieve pain and heal soft tissues of the body. The electrical current used in Microcurrent Therapy is so small that it is rarely felt.