Description
GenuFIT
Knee orthosis with articulated rods
Description
Class I Medical Device (Directive 93/42/EEC).
Opening knee pad in AirX fabric.
The ultra-flat anatomical design allows good flexibility of movement with optimal adaptation to the joint.
Breathable AirX fabric construction.
Popliteal insert (without central seam) in soft Soft-X fabric for greater comfort.
Polycentric articulated rods with very low profile, with the possibility of limiting flexion to 60°, 90°.
New softer and more elastic edge.
New split front opening for easy donning: internal central pre-fixing closure and external definitive fastening closure. Opening for the kneecap.
Renewed closure system (European patent EP 2215993 B1): stabilizing straps with buckles and elastic insert, for optimal adjustment of the thrust.
Indications: gonarthrosis or sequelae of sprain trauma with residual instability of the collaterals (non-operable knee).
How to use
- First application for the doctor/technician
1. Open all the Velcro straps and temporarily close them on themselves.
2. Wrap the brace around the knee, with the orange label facing upwards, centering the opening on the kneecap and close the positioning Velcro straps above and below the knee, first the central ones, then the external ones.
3. If necessary, remove the knee brace, slide the rods out of the pockets and shape them to fit the shape of your leg. Then reinsert the rods into the pockets and reapply the knee brace.
4. Insert the two Y-shaped ends of the upper strap into the corresponding ring, pull symmetrically with both hands and secure with Velcro. Repeat the operation with the lower strap.
5. If necessary, you can shorten the straps:
remove the Y-shaped Velcro at the end of the strap; cut off the excess strap; reapply the Y-shaped Velcro.
- Subsequent applications
1. Open all the Velcro straps and temporarily close them on themselves.
2. Wrap the brace around the knee, with the orange label facing upwards, centering the opening on the kneecap and close the positioning Velcro straps above and below the knee, first the central ones, then the external ones.
3. Insert the two Y-shaped ends of the upper strap into the corresponding ring, pull symmetrically with both hands and secure with Velcro. Repeat the operation with the lower strap.
Cleaning and maintenance
After removing the temples, hand wash up to 30°C with neutral soap. Leave to dry away from heat sources.
Do not bleach. Do not iron. Chemical cleaning not allowed. Do not tumble dry.
Warnings
It is recommended that the pressure exerted by the device does not act on parts of the body that have wounds, swelling or tumefaction. It is advisable not to over-tighten the product so as not to generate areas of excessive local pressure or compression of nerves and/or underlying blood vessels. If in doubt about how to apply it, contact an orthopedic technician. Carefully read the composition of the product on the internal label. It is advisable not to wear the device near open flames or strong electromagnetic fields. The product, designed for the specific indications listed below, must be prescribed by a doctor and applied by an orthopedic technician, who is the competent reference figure both for the application and for information regarding safe use, in accordance with individual needs. To ensure its effectiveness, tolerability and correct functioning, the application must be carried out with the utmost care. Any modification to the structure or adjustment of the device must be prescribed by a doctor and performed by an orthopedic technician. Do not alter the adjustment made by the doctor/orthopedic technician under any circumstances. The manufacturer's liability lapses in the event of inappropriate use or adaptation. The orthosis is designed for use by a single patient; otherwise the manufacturer declines all liability, in accordance with the provisions of the regulation for medical devices. In hypersensitive subjects, direct contact with the skin may cause redness or irritation. In the event of pain, swelling, tumefaction or any other abnormal reaction, contact your doctor immediately. The orthopedic effectiveness of the product is guaranteed only with the use of all its components.
Format
Length: 34 cm.
Cod. PR3G1115A
Class I Medical Device (Directive 93/42/EEC).
Opening knee pad in AirX fabric.
The ultra-flat anatomical design allows good flexibility of movement with optimal adaptation to the joint.
Breathable AirX fabric construction.
Popliteal insert (without central seam) in soft Soft-X fabric for greater comfort.
Polycentric articulated rods with very low profile, with the possibility of limiting flexion to 60°, 90°.
New softer and more elastic edge.
New split front opening for easy donning: internal central pre-fixing closure and external definitive fastening closure. Opening for the kneecap.
Renewed closure system (European patent EP 2215993 B1): stabilizing straps with buckles and elastic insert, for optimal adjustment of the thrust.
Indications: gonarthrosis or sequelae of sprain trauma with residual instability of the collaterals (non-operable knee).
How to use
- First application for the doctor/technician
1. Open all the Velcro straps and temporarily close them on themselves.
2. Wrap the brace around the knee, with the orange label facing upwards, centering the opening on the kneecap and close the positioning Velcro straps above and below the knee, first the central ones, then the external ones.
3. If necessary, remove the knee brace, slide the rods out of the pockets and shape them to fit the shape of your leg. Then reinsert the rods into the pockets and reapply the knee brace.
4. Insert the two Y-shaped ends of the upper strap into the corresponding ring, pull symmetrically with both hands and secure with Velcro. Repeat the operation with the lower strap.
5. If necessary, you can shorten the straps:
remove the Y-shaped Velcro at the end of the strap; cut off the excess strap; reapply the Y-shaped Velcro.
- Subsequent applications
1. Open all the Velcro straps and temporarily close them on themselves.
2. Wrap the brace around the knee, with the orange label facing upwards, centering the opening on the kneecap and close the positioning Velcro straps above and below the knee, first the central ones, then the external ones.
3. Insert the two Y-shaped ends of the upper strap into the corresponding ring, pull symmetrically with both hands and secure with Velcro. Repeat the operation with the lower strap.
Cleaning and maintenance
After removing the temples, hand wash up to 30°C with neutral soap. Leave to dry away from heat sources.
Do not bleach. Do not iron. Chemical cleaning not allowed. Do not tumble dry.
Warnings
It is recommended that the pressure exerted by the device does not act on parts of the body that have wounds, swelling or tumefaction. It is advisable not to over-tighten the product so as not to generate areas of excessive local pressure or compression of nerves and/or underlying blood vessels. If in doubt about how to apply it, contact an orthopedic technician. Carefully read the composition of the product on the internal label. It is advisable not to wear the device near open flames or strong electromagnetic fields. The product, designed for the specific indications listed below, must be prescribed by a doctor and applied by an orthopedic technician, who is the competent reference figure both for the application and for information regarding safe use, in accordance with individual needs. To ensure its effectiveness, tolerability and correct functioning, the application must be carried out with the utmost care. Any modification to the structure or adjustment of the device must be prescribed by a doctor and performed by an orthopedic technician. Do not alter the adjustment made by the doctor/orthopedic technician under any circumstances. The manufacturer's liability lapses in the event of inappropriate use or adaptation. The orthosis is designed for use by a single patient; otherwise the manufacturer declines all liability, in accordance with the provisions of the regulation for medical devices. In hypersensitive subjects, direct contact with the skin may cause redness or irritation. In the event of pain, swelling, tumefaction or any other abnormal reaction, contact your doctor immediately. The orthopedic effectiveness of the product is guaranteed only with the use of all its components.
Format
Length: 34 cm.
| Cut | Thigh circumference |
| XS | 33-39 cm |
| S | 39-45 cm |
| M | 45-52 cm |
| THE | 52-58 cm |
| XL | 58-66 cm |
| XXL | 66-75 cm |
Cod. PR3G1115A
