Taking Off The Socket And Liner; Legal Information; Trademarks; Technical Data - Ottobock 5A60-Varos Instrucciones De Uso

6.2 Taking off the socket and liner

1) Pull the Boa dials away from the socket.
2) Pull the outer socket shell (lateral) to the outside.
If plastic adhesive strips are used in the lateral socket shell, pull until there is no longer any
contact between the plastic adhesive strips and textile cover of the liner.
3) Push the socket off the residual limb.
In doing so, preferably grasp the socket brim of the lateral socket shell with one hand and the
socket brim of the medial socket shell with the other hand.
4) Unroll and remove the liner from the residual limb.
7 Cleaning
1) Clean the product with a damp cloth and mild soap (e.g. Ottobock 453H10=1 Derma Clean)
when needed.
2) Dry the product with a lint-free cloth and allow it to air dry fully.
The socket brim pad can be removed for cleaning.
1) Clean the socket brim pad with water and mild soap (e.g. 453H10=1 Ottobock Derma Clean)
when needed.
2) Dry the socket brim pad with a lint-free cloth and allow it to air dry fully.
3) After it is completely dried, attach the socket brim pad to the medial socket shell again.
8 Maintenance
► A visual inspection and functional test of the prosthetic components should be performed
after the first 30 days of use.
► Conduct annual safety inspections.

9 Legal information

9.1 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.

9.2 Trademarks

All product names mentioned in this document are subject without restriction to the respective
applicable trademark laws and are the property of the respective owners.
All brands, trade names or company names may be registered trademarks and are the property of
the respective owners.
Should trademarks used in this document fail to be explicitly identified as such, this does not justi­
fy the conclusion that the denotation in question is free of third-party rights.
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.

10 Technical data

Ambient conditions
Transport in original packaging -25 °C/-13 °F to +70 °C/+158 °F
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