bioMetric SpinalPak Kompletny podręcznik - Strona 18

Przeglądaj online lub pobierz pdf Kompletny podręcznik dla Sprzęt medyczny bioMetric SpinalPak. bioMetric SpinalPak 20 stron. Non-invasive spine fusion stimulator system

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Patient Counseling Information

The patient should be thoroughly instructed on how to properly use and care for the

Non-invasive Spine Fusion Stimulator System and receive the Patient Manual, which provides detailed

instructions. A summary of the key points in the patient labeling is provided below.

Compliance -

T he patient should be instructed that compliance with device use and care is critical

to assure the proper function of the device and effective treatment.

Battery Pack -

T he patient should be instructed to insert a fully charged battery pack into the

stimulator every 24 hours.

Electrodes -

T he patient should be instructed to replace the electrodes when needed, and

to clean the electrode sites thoroughly with soap and water prior to applying

the electrodes.

Skin Irritation -

T he patient should be instructed to examine the skin for irritation when replacing

the electrodes. If irritation is present, the patient should be instructed to relocate the

electrodes adjacent to the original sites. The patient should be evaluated periodically

to assess the skin for sensitivity.

Alarms -

S ee LCD Symbol Descriptions and Instructions (page 9). The patient should be

instructed to keep the audible alarm system engaged as often as practical, and to

engage the alarm system if it has been disengaged as soon as practical.

Bathing -

T he patient should be instructed to disconnect the stimulator during bathing,

showering or swimming. It should be reconnected as soon as practical

following these activities. The patient should also be instructed to either remove

the electrodes, or to cover the electrodes with the protective retainer patches,

during showering.

Storage and Handling

The

Biomet

SpinalPak

dry place. The device components should be handled with care. Damage may occur if the device is

inappropriately handled or abused.

Disposal Instructions

When treatment has concluded as determined by the prescribing physician (see page 10), Biomet

requests that the patient disposes of the

System according to local statutes and regulations.

Non-invasive Spine Fusion Stimulator System should be stored in a cool and

Non-invasive Spine Fusion Stimulator

Biomet

SpinalPak

Biomet

SpinalPak