Relative Contraindications - Juzo Easy Fit Instrucciones De Uso

Ocultar thumbs Ver también para Easy Fit:
Tabla de contenido

Publicidad

Idiomas disponibles
  • ES

Idiomas disponibles

  • ESPAÑOL, página 14
Safety notice
The donning and doffing aid should be dispensed by pro-
perly trained staff only, at a medical retailer. Please cont-
act your specialist retailer in the event of damage. Do not
repair the product yourself – this may affect its quality and
medical effectiveness. Only use the donning and doffing
aid when sitting. Carefully read the instructions for use
and follow them. Keep the instructions in a safe place. The
manufacturer does not accept any liability for damage/in-
juries resulting from improper use or misuse. Store Juzo
Easy Fit away from children. Only ever use Juzo Easy Fit if
the frame and the clasp are in perfect condition.
Cleaning
Wipe the product with a damp cloth and conventional
household cleaner.
Material and technical data
Technical data
Item number: 1890
Dimensions:
a) 32.0 cm
b) 52.0 cm
c) 28.5 cm
d) 18.0 cm
Frame material: Metal, coated
Clasp material: PVC
Indications
∙ Paralysis
∙ Age-related reduction in strength
∙ Osteoarthritis/rheumatism
∙ Morbid obesity
∙ Extensive stiffening of the spine/hip/knee
∙ Degenerative disorders of the hands/in the area of the
hand
∙ Consequence of injuries/amputations

Relative contraindications

Absolute immobility
Liability for failure to comply with this contraindication
cannot be accepted by the Julius Zorn GmbH Group.
Side effects
There are no known side effects when this product is used
correctly. However, if you notice any adverse changes
during the prescribed use, please consult your doctor or
medical retailer immediately. The manufacturer does not
accept any liability for damage/injuries resulting from im-
proper use or misuse. In the event of complaints related to
this product, please contact the medical retailer directly.
Only serious incidents that may lead to a major deteriorati-
on in the patient's medical condition or to death should be
reported to the manufacturer and the relevant authority in
the Member State. Serious incidents are defined in Article
2 (65) Regulation (EU) 2017/745 (MDR).
Disposal
Disposal regulations may vary depending on your country.
Therefore, please follow the national guidelines in the
relevant country.
EN

Publicidad

Tabla de contenido
loading

Tabla de contenido