INTELECT RPW-2
Product Description
The Intelect RPW 2 device is intended to be used as a therapeutic modality by clinicians needing to provide patients with a powerful and proven method of treating indications as pain, myofascial trigger points, disorders of tendon insertions, activation of muscle and connective tissue. The device is intended to be operated in a clinical environment, it can be moved from room to room. The device is not intended to be regularly transported from one facility to another. It is not intended for home use.
- Promotes blood flow through the tissue and boosting metabolism.
- Soothing relief from muscle strain and stress.
- Plantar Fasciitis is an inflammatory condition of the foot caused by excessive wear to the plantar facia that supports the arch
- Shoulder calcifications and chronic shoulder pain
- Tennis elbow, inflammation of tendon attachments on cubital or radial part of elbow joint (humeral)
- Pain due to inflammation of the Achilles tendon or the bursa associated with it.
- Pain in the front of, behind, and around the kneecap.
- Localizing and Deactivatiing Trigger Points
- Activation of Muscle and Connective Tissue
- Increasing Circulation
- Pulse vibration Massage
- Disorder of Tendon Insertions
2174KIT Intelect RPW 2 230V unit set including standard accessories
2173KIT Intelect RPW 2 120V unit set including standard accessories
2175KIT Intelect RPW 2 100V unit set including standard accessories
2174: 230V AC 50-60Hz 350VA
2173: 120V AC 50- 60Hz 350VA
2175: 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, 800×480 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