I. General safety and use of the product.
II. Intended use of the product.
The prophylac�c-rehabilita�on chair is intended for people with back injuries and with lumbar pain
syndromes. The task of the chair is to relieve the intervertebral discs and back muscles in a si�ng posi�on.
It also fulfills a preven�ve task in shaping the correct posture during long-term si�ng work. Due to to the
mul�-stage adjustment system, it allows you to assume a convenient posi�on for people of various height.
People with other spine condi�ons or in case of any doubts are advised to consult a specialist doctor or
chiroprac�c.
III. Cleaning and maintenance.
The metal frame should be cleaned with a damp cloth and mild cleaning agents. Upholstered elements should
be cleaned with generally available agents intended for cleaning upholstery. Do not use harsh chemicals.
IV. Safety condi�ons for the assembly.
1. Before use, make sure that all components are properly a�ached and �ghtened.
2. The chair should be folded by adults.
3. In caseof finding any defects, immediately contact the manufacturer and do not use the chair un�l the
defect is removed.
V. Construc�on and technical data.
Product components:
1. Frame – strong and durable made of carbon steel covered with a varnish coa�ng.
2. Seat and knee support - made of 20 [mm] plywood and 75 [mm] polyurethane foam covered with a
pleasant-to-touch so� and breathable PU material.
3. Two-stage regula�on system based on pneuma�c rod Ø80 [mm]:
- for the knee sec�on in the range of 0-30 [°];
- for the seat in the range of 0-24 [°].
4. Automa�c backrest adjustment depending on the user's posi�on.
5. Wheels with an addi�onal PU layer and a locking system.
1. Please read the User Manual before using the product.
2. Place the product on a flat surface before use.
3. Before using, make sure that the product does not wave or �lt.
4. Do not use the product if product components are malfunc�oning or damaged.
5. Do not stand or jump on the product.
6. Do not put fingers or other body parts into the opera�ng area of the adjustment mechanism.
7. Do not expose the product to strong sunlight.
8. Do not use the product in extreme temperature and humidity condi�ons.
9. Use the product only for its intended purpose.
10. Do not make any modifica�ons or repairs to the product.
11. Only a�er mee�ng the above recommenda�ons there are no contraindica�ons to use the
product.
12. Each serious incident related to the device should be reported to the manufacturer and the
Office for Registra�on of Medicinal Products, Medical Devices and Biocidal Products.
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