Product Description - Ottobock AxonCharge Integral 757L500 Instrucciones De Uso

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2 Product Description

2.1 Function
The AxonCharge Integral 757L500 is designed to charge the AxonEnergy Integral or 757B501 in
the Ottobock Axon-Bus prosthetic system.
Charging is performed automatically after the charging plug has been connected to the charging
receptacle of the Axon-Bus prosthetic system. The charging plug is secured to the charging
receptacle by the integrated magnet. The special contours of the charging receptacle and char­
ging plug ensure quick, reliable positioning of the two components. LEDs indicate the readiness
of the battery charger and the current battery charge level.
3 Application
3.1 Intended Use
The AxonCharge Integral 757L500 is intended solely for charging of the AxonEnergy Integral
757B500 or 757B501.
3.2 Use / Field of Application
The 757L500 AxonCharge Integral can be used to charge unilateral or bilateral prosthetic fittings
of the upper limbs.
3.3 Conditions of Use
The 757L500 AxonCharge Integral must be used in closed rooms only.
3.4 User/Qualifications
The 757L500 AxonCharge Integral may only be used by persons who have previously been
instructed in its proper use.
4 Safety
4.1 Explanation of Warning Symbols
Warning regarding possible serious risks of accident or injury.
WARNING
Warning regarding possible risks of accident or injury.
CAUTION
Warning regarding possible technical damage.
NOTICE
4.2 General Safety Instructions
WARNING
Use of damaged power supply unit, adapter plug or battery charger
Risk of electric shock due to contact with exposed, live components.
Do not open the power supply unit, adapter plug or battery charger.
Do not expose the power supply unit, adapter plug or battery charger to extreme loading
conditions.
Immediately replace damaged power supply units, adapter plugs or battery chargers.
WARNING
Operating the product near active implanted systems
Interference with active implantable systems (e.g., pacemaker, defibrillator, etc.) due to electro­
magnetic interference of the product.
When operating the product in the immediate vicinity of active implantable systems, ensure
that the minimum distances stipulated by the manufacturer of the implant are observed.
10 | Ottobock

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