Legal Information - Ottobock 8165 Genu Neurexa Instrucciones De Uso

→ The centre of the orthotic joint should be at the height of the middle of the patella.
→ The orthosis should not be twisted on the leg.
→ The straps should be tight but not impair the patient's comfort.
Inform the patient:
Inspect the orthosis for damage
► Inspect the orthosis for damage daily. Contact the qualified personnel promptly if changes are
noted.
5 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 orthosis regularly:
► NOTICE! Detergent residues may cause skin irritation and wear of material.
1) Remove all metal splints.
2) Fasten all hook-and-loop closures.
3) Recommendation: Use a laundry bag or net.
4) Wash the orthosis in warm water at 30 °C with standard mild detergent. Do not use fabric
softener. Rinse thoroughly.
5) Allow to air dry. Do not expose to direct heat sources (e.g. sunlight, stove or radiator).
6) Reinsert the metal splints.
1) Take the bars out of the pockets.
2) Fasten all hook-and-loop closures.
3) Recommendation: Use a laundry bag or net.
4) Wash the orthosis in warm water at 30 °C with standard mild detergent. Do not use fabric
softener. Rinse thoroughly.
5) Allow to air dry. Avoid exposure to direct heat (e.g. sunlight, oven or radiator).
6) Reinsert the bars into the orthosis.
6 Disposal
Dispose of the product in accordance with national regulations.

7 Legal information

All legal conditions are subject to the respective national laws of the country of use and may vary
accordingly.
7.1 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.
7.2 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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