11
Adjusting the flexion position and abduction
>
Prerequisite:
The product has been applied to the patient.
1) The leg positioning shells are connected to the trunk brace. Open the clip fasteners of the
shoulder harness one after the other and adjust the leg flexion position by changing the length
of the orthosis (see fig. 6).
2) Adjust the abduction of the leg positioning shells with the turnbuckle. Loosen the right-hand
counter nut and rotate the turnbuckle to adjust the width with the threaded bar (see fig. 6).
Secure the desired position with the left-hand counter nut.
6.2 Removal
1) Open the chest strap.
2) Open the two clip fasteners of the trunk brace and place it over the shoulders.
3) Open the 4 hook-and-loop straps on the two leg positioning shells.
7 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.
►
Allowable cleaning agent:
pH neutral soap (e.g. 453H10 Derma Clean)
1) Clean the product with clear fresh water.
2) Rinse the product thoroughly.
3) Dry with a soft, lint-free cloth.
4) Allow to air dry in order to remove residual moisture. Do not expose to direct heat sources
(e.g. sunlight, stove or radiator).
8 Disposal
Dispose of the product in accordance with national regulations.
9 Legal information
All legal conditions are subject to the respective national laws of the country of use and may vary
accordingly.
9.1 Local Legal Information
Legal information that applies
exclusively
to specific countries is written in the official language
of the respective country of use after this chapter.
9.2 Liability
The manufacturer will only assume liability if the product is used in accordance with the descrip
tions and instructions provided in this document. The manufacturer will not assume liability for
damage caused by disregarding the information in this document, particularly due to improper
use or unauthorised modification of the product.
9.3 CE conformity
This product meets the requirements of the European Directive 93/42/EEC for medical devices.
This product has been classified as a class I device according to the classification criteria out
lined in Annex IX of the directive. The declaration of conformity was therefore created by the man
ufacturer with sole responsibility according to Annex VII of the directive.
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