BIOSWING Propriomed® 2
Product features Haider Bioswing Propriomed 2:
– Length: 165 cm
– Weight: 920 g
– Vibration frequency: 4.0 – 5.2 Hz
– Max. Permissible vibration range: 60 cm
– Red color
Haider Bioswing Propriomed 2
The therapeutic oscillating rod has a frequency spectrum of 4.0 to 5.2 Hz and is thus suitable for motorized well-coordinated patients. To adjust the frequency, move the frequency controls to appropriate positions. A comprehensive exercise manual with exercises is included in the scope of delivery.
The oscillating rod is made of high-quality valve spring steel for load-bearing vibrations up to a maximum of 60 cm. Should the vibration range be achieved permanently with the exercises, we recommend using a shorter rod with a more intense effect. The hygienic plastic handle is antiallergic and can be disinfected with disinfecting pieces.
Difference of different models
The oscillating rods differ in length and thus also in their oscillation frequency. The longer the oscillating rod, the easier the exercises for the back and the depth musculature. While the handle of the two models is made of plastic, the handle of the 100 model is made of powder-coated aluminium. In addition, the small staff is also used in children’s rehabilitation.
How does the Propriomed vibrator work?
The swing with the Propriomed leads to training effects in several body systems. Doses rhythmic stimuli dynamically activate the synergistic muscle groups and the neuromuscular action and reaction time is improved besides the holding function. The muscles in the arms, shoulder girdles, back and the entire trunk and in the lap belt are stimulated as far as the thighs and their metabolism is optimized. With the exercises not only the motor control can be improved, but also the elasticity of the connective tissue and the regulation of the vegetative nervous system.
Other proprioceptive vibratory rods such as the Bioswing Improve 150 or the simple design as a Flexi-Bar oscillating rod can be found in our online shop category Proprioceptive devices.
| Product meets the requirements of the Medical Product Act (MPG)Classification according to Directive 93/42 / EEC:Class I |



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