bioMetric SpinalPak 전체 매뉴얼 - 페이지 5

{카테고리_이름} bioMetric SpinalPak에 대한 전체 매뉴얼을 온라인으로 검색하거나 PDF를 다운로드하세요. bioMetric SpinalPak 20 페이지. Non-invasive spine fusion stimulator system

Biomet

SpinalPak

Caution: Federal Law (U.S.A.) restricts this device to sale by or on the order of a physician.

Rx Only.

This device is not intended for re-sale or re-distribution. Single patient use.

The Biomet

SpinalPak

by inducing a low electrical current at the fusion site. The therapeutic signal generates a low energy

electrical field by passing a specific current between the electrodes.

ELECTRICAL REQUIREMENTS FOR BATTERY AND CHARGER

Charger

Input: 100-240 VAC 50/60 Hz 6 W

Output: 12V DC 500mA

F or use with the Biomet

only (PN 1067720).

Battery rating: 3.7 VDC > 800 mAh

Do not use the battery pack supplied with this unit in any other device. Use of the Biomet

Non-invasive Spine Fusion Stimulator System battery pack in any other device may cause damage or

malfunction to the battery pack and/or device.

System Components

STIMULATOR

Biomet

SpinalPak

The

which allows for ambulatory use. It includes an audible and visible self-checking alarm mechanism to alert the

patient if it is not functioning properly. The

is designed to store the patient's daily therapeutic treatment data which may be downloaded and read with the

patient compliance software (See Patient Compliance Monitoring Page 10). Patients are encouraged to bring the

stimulator to each follow-up visit with the prescribing physician to review how they are using their stimulator.

Non-invasive Spine Fusion Stimulator System

Non-invasive Spine Fusion Stimulator System (Figure 1) promotes healing

SpinalPak

Non-invasive Spine Fusion Stimulator System battery pack

Non-invasive Spine Fusion Stimulator System operates on a rechargeable battery pack,

Biomet

Figure 1

SpinalPak

Non-invasive Spine Fusion Stimulator System

SpinalPak