Otto Bock 50R301N Dyneva light, Instructions For Use Manual, Page: 15 / 112

15
CAUTION
Incorrect or excessively tight application
Risk of local pressure and constriction of blood vessels and nerves due to improper or exces­
sively tight application
►
Ensure that the product is applied properly and fits correctly.
NOTICE
Use of a worn or damaged product
Limited effectiveness
► Before each use, check the product for functional reliability and for possible wear or dam­
age.
►
Do not continue using a product that is no longer functional, or that is worn or damaged.
1) Open the brace strap on one side.
2) Position the brace frame so that the bottom pad is positioned at the level of the sacrum and
the two upper pads below the shoulder blades.
3) Centre the abdominal pad.
4) Use the redirection mechanism of the spring to evenly adjust the length of the straps.
NOTICE! Make sure that the angle of the spring does not exceed 20°.
6 Cleaning
NOTICE
Use of improper cleaning agents
Damage to the product due to use of improper cleaning agents
►
Only clean the product with the approved cleaning agents.
Clean the brace regularly:
1) Fasten all hook-and-loop closures.
2) Hand-wash the straps and pads in warm water at
30 °C (86 °F)
using ph-neutral detergent.
Rinse thoroughly.
3) Allow to air dry. Do not expose to direct heat sources (e.g. sunlight, stove, or radiator).
4) Clean contamination off the brace frame with a moist cloth and allow to air dry.
7 Disposal
Dispose of the product in accordance with national regulations.
8 Legal Information
All legal conditions are subject to the respective national law of the country of use and may vary
accordingly.
8.1 Liability
The manufacturer shall be liable in the event that the product is used in accordance with the
descriptions and instructions in this document. The manufacturer will not assume liability for dam­
age caused by disregarding the information in this document, particularly due to improper use or
unauthorized modification of the product.
8.2 CE Conformity
The product meets the requirements of Regulation (EU) 2017/745 on medical devices. The CE
declaration of conformity can be downloaded from the manufacturer's website.