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SHOCKWAVE INTELECT RPW 2
The Intelect® RPW 2 from Chattanooga allows for the treatment of indications with radial, pneumatically-generated, low-energy acoustic waves, or ‘pressure pulses’. The applied pressure pulse propagates radially within the tissue, generating a therapeutic effect.
We have Special Offer packages at times on Shockwave. Drop an email to matt@sportsphysio.ie for details and more information on the specification and full training we provide .
Availability:
In stock
SKU
150-527
The Intelect® RPW 2 from Chattanooga allows for the treatment of indications with radial, pneumatically-generated, low-energy acoustic waves, or ‘pressure pulses’. The applied pressure pulse propagates radially within the tissue, generating a therapeutic effect.
The V-ACTOR® HF optional hand piece allows mechanical vibration, for vibration massage.
INDICATIONS
• ACHILLES TENDINOPATHY
• DISORDERS OF TENDONS INSERTIONS
• MYOFASCIAL TRIGGER POINTS
• PAIN & INFLAMMATION IN ORTHOPAEDIC CONDITIONS
• PLANTAR FASCIITIS
• PULSE VIBRATION MASSAGE
RECOMMENDED TREATMENT GUIDELINES
• LOCALIZE THE PAINFUL AREAS YOU PLAN TO TREAT
• SELECT MOST APPROPRIATE TRANSMITTERS BASED ON TREATMENT GOAL AND TARGETED TISSUE
• APPLY ULTRA SOUND WATER BASED GEL ON THE SKIN OVERLYING THE TREATMENT AREA
• ALWAYS START WITH LOWER LEVEL OF INTENSITY
• PERFORM A POST-TREATMENT TEST TO SEE FOR BETTER FUNCTION AND DECREASED IN PAIN
TECHNICAL INFORMATION
174: 230V AC 50-60Hz 350VA
173: 120V AC 50- 60Hz 350VA
175: 100V AC 50-60Hz 400VA
DIMENSIONS
WxHxD: 410x1100x425mm
WEIGHT: 30kg
COMPRESSED AIR OUTPUT: 0.3-5.0 bar
POWER INCREMENT SETTINGS: 0.1 bar
PULSE AMPLITUDE: Approx 2mm at 3 bar, idling (without coupling)
PULSE WIDTH: Approx 6-12ms
PULSE FREQUENCY: FALCON® handpiece 1-21Hz for RPW, V-ACTOR® handpiece 1-50Hz for vibration
MODE: Single pulse or continuous
USER INTERFACE: 7 inch, 800x480 pixels color graphic capacitive touch screen
CONFORMITY: This device complies with the applicable standards EN/IEC 60601-1, CAN/CSA-C22.2 No.601.1, UL Std. No 60601-1.
CLASSIFICATION ACCORDING TO MDD: class IIa device 93/42 60601-1
LEGAL MANUFACTURER: DJO France SAS - CE 2797
