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LTV 1200 Operator's Manual - AARC.org

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Notices<br />

The <strong>LTV</strong> ® <strong>1200</strong> or 1150 ventilator complies with limitations as specified in IEC 601-1-2 for Medical<br />

Electrical Equipment. It does however, use and radiate radio frequency energy.<br />

The function of this machine may be adversely affected by the operation of other nearby equipment,<br />

such as high frequency surgical diathermy equipment, short-wave therapy equipment, defibrillators,<br />

or MRI equipment (except the MR Conditional <strong>LTV</strong> ® <strong>1200</strong>).<br />

The <strong>LTV</strong> ® <strong>1200</strong> and 1150 ventilator may emit and receive electromagnetic interference. Avoidance of<br />

this exposure is recommended whenever possible.<br />

The MR Conditional <strong>LTV</strong> ® <strong>1200</strong> System is comprised of only (i.e., no unauthorized accessories): an<br />

MR Conditional <strong>LTV</strong> ® <strong>1200</strong> ventilator (P/N 18888-2XX), <strong>LTV</strong> ® <strong>1200</strong> MR Safe 15ft Patient Circuit (P/N<br />

19189-001), MR Conditional Floor Stand (P/N 14982-001), and an <strong>LTV</strong> ® AC adapter (P/N 18053-<br />

001).<br />

The MR Conditional <strong>LTV</strong> ® <strong>1200</strong> System is suitable for use in both 1.5 and 3.0 Tesla (not to exceed<br />

3.0 Tesla static magnetic field) shielded magnetic scanners (see Chapter 16 – MR Conditional<br />

System for more information).<br />

To ensure that your use of the <strong>LTV</strong> ® <strong>1200</strong> MR Conditional System results in images that are free of<br />

an unacceptable artifact, the <strong>LTV</strong> ® <strong>1200</strong> MR Conditional System should be tested prior to initial<br />

clinical use (utilizing a suitable phantom) in each intended use MR environment utilizing the ventilator<br />

power source (AC Adaptor or SprintPack Lithium-ion Power System) that will be selected for use.<br />

European Regulatory Requirements per 93/42/EEC Medical Device Directives<br />

CareFusion European Representative for vigilance reporting within the European Community is:<br />

CareFusion Germany 234 GmbH<br />

Leibnizstrasse 7<br />

97204 Hoechberg, Germany<br />

Main Office: 49.931.4972.0<br />

Fax: 49.931.4972.423<br />

Email: support.vent.eu@carefusion.com<br />

Any product malfunctioning issues that fall under Medical Device Directives Essential Requirements<br />

should be directed to CareFusion Germany 234 GmbH.<br />

Operator’s <strong>Manual</strong> <strong>LTV</strong> ® <strong>1200</strong> / 1150 Ventilators Page iii<br />

P/N 19802-001 Rev. F

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