Cleaning And Care; Legal Information - Ottobock Liner Gebrauchsanweisung

2) Roll up the liner and place it on the end of the residual limb.
NOTICE! Align a distal connecting element (e.g. pin, metal
cap) with the longitudinal axis of the residual limb.
3) Unroll the liner onto the residual limb so that it has no wrinkles or
air inclusions, without shifting the soft tissue.
4) Check the fit and the alignment of the liner.
INFORMATION: TF liners are not permitted to end inside the
prosthetic socket.
Doffing
1) Roll up the liner and remove it from the residual limb.
2) Recommendation: Clean the liner (see Page 10).

6.2 Cleaning and Care

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.
INFORMATION
Clean the liner and skin more frequently in case of increased per­
spiration. Wearing a liner requires daily intensive skin care.
Ottobock recommends the use of the Derma skin care system.
1) Turn the liner inside out.
2) Hand wash the liner in warm water (30 °C) using neutral deter­
gent (e.g. Ottobock 453H10=1 Derma Clean).
3) Thoroughly rinse the liner with clear water until all detergent
residues have been removed.
4) Turn the liner again so the outer side/textile material is on the out­
side.
10
5) Put a hand towel into the liner and leave the liner to dry lying flat
on a drying rack. Alternatively, use a drying stand (TT: 5Y100=1
TF: 5Y100=2).
NOTICE! Liner with textile cover: To avoid damaging the
liner, dry it with the textile material on the outside.
7 Disposal
This product may not be disposed of with regular domestic waste in
all jurisdictions. Disposal that is not in accordance with the regula­
tions of the country where the product is used may have a detrimental
impact on health and the environment. Please observe the information
provided by the responsible authorities in the country of use regarding
return, collection and disposal procedures.

8 Legal information

All legal conditions are subject to the respective national laws of the
country of use and may vary accordingly.
8.1 Liability
The manufacturer will only assume liability if the product is used in
accordance with the descriptions 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.
8.2 CE conformity
The product meets the requirements of Regulation (EU) 2017/745on
medical devices. The CE declaration of conformity can be down­
loaded from the manufacturer's website.
8.3 Warranty
The manufacturer warrants this device from the date of fitting. The
warranty covers defects that can be proven to be a direct result of
flaws in the material, production or construction and that are reported
to the manufacturer within the warranty period.
Further information on the warranty terms and conditions can be
obtained from the competent manufacturer distribution company.