Changing The 8E33=7*, 8E33=9* Terminal Device; Legal Information - Ottobock 8E33 Serie Instrucciones De Uso

7.4 Changing the 8E33=7*, 8E33=9* terminal device

Separating the terminal device from the socket
1) Rotate the terminal device once around its own axis until a slight resistance is felt (about
360°).
2) Overcome this resistance and pull the terminal device off the socket.
Attaching the terminal device to the socket
1) Insert the quick-disconnect wrist unit into the lamination ring and press it in firmly.
2) Turn the terminal device slightly to the left or right.
3) Verify proper attachment by pulling on the terminal device.
8 Cleaning
NOTICE
Improper product care
Damage to the product due to the use of incorrect cleaning agents.
► Only clean the product with a damp cloth and mild soap (e.g. 453H10=1 Ottobock Der­
maClean).
1) Clean the product with a damp cloth and mild soap (e.g. Ottobock 453H10=1 Derma Clean)
when needed.
Ensure that no liquid penetrates into the system component(s).
2) Dry the product with a lint-free cloth and allow it to air dry fully.
9 Maintenance
Since all moving mechanical parts are subject to wear, regular service inspections are recom­
mended. These service inspections include an inspection of the product and, when necessary,
the replacement of wear parts.

10 Legal information

10.1 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 disregard of this document, particularly due to improper use or unauthorised
modification of the product.
10.2 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.
10.3 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.
The product meets the requirements under the RoHS Directive 2011/65/EU of the European Par­
liament and of the Council of 8 June 2011 on the restriction of the use of certain hazardous sub­
stances in electrical and electronic equipment.
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