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Wechselwirkungen machen eine Betrachtung der MR-Sicherheit für den Hersteller u. 6 Jan 2021 ISO/TS 10974 describes the most significant hazards for patients resulting from scanner-device interactions: heating of the device via ISO/TS 10974:— , Assessment of the safety of magnetic resonance imaging for patients with an active. implantable medical device. IEC 60601-1:2005+A1: 2012, ISO/TS 10974:2018. Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device. International Standards Passive Medical Devices and issues about the MR worker (IEC 60601-2-33 3 rd edition) as well as introducing ISO/TS 10974 for active implants.

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5350. 1/1640 - ISO/IEC 9945 1/1641 - ISO/TS16949 1/1642 - ISO/TS 16949 1/1643 8/10972 - Inferiolabiata spinosa 8/10973 - Inferior 8/10974 - Inferior gemellus Maj:ts orden 4/5774 - Vapenoffer 4/5775 - Vapenpolitik 4/5776 - Vapenrock 8/10973 - Venus från Trasimeno 8/10974 - Venus från Vinča 8/10975 - Venus från Volmar Yxkull 20/26089 - Volmari Iso-Hollo 20/26090 - Volmarstein 20/26091 ISO/TS 10974:2018 is applicable to implantable parts of active implantable medical devices (AIMDs) intended to be used in patients who undergo a magnetic resonance scan in 1,5 T, cylindrical (circular or elliptical cross-section) bore, whole body MR scanners operating at approximately 64 MHz with whole body coil excitation.

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ISO TS 10974, 1st Edition, May 2012 - Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device intended to be used in patients who undergo a magnetic resonance scan in 1,5 T, cylindrical (circular or elliptical cross-section) bore, whole body MR scanners operating at approximately 64 MHz with whole body coil excitation. ISO/TS 10974 is a test specification used for assessing the safety of magnetic resonance imaging for patients with an active implantable medical device (AIMD). An “active medical device” refers to an electrically active device that is surgically or medically introduced into the human body that remains in place after the procedure. While the scope of ISO/TS 10974 is AIMDs, it 109 contains detailed information about hazards for medical devices in the MR environment 110 and methods for assessing specific hazards that can be ISO TS 10974 Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device PD ISO-TS 10974-2018.

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ISO TS 10974 April 1, 2018 Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device intended to be used ISO/TS 10974:2018 is applicable to implantable parts of active implantable medical devices (AIMDs) intended to be used in patients who undergo a magnetic resonance scan in 1,5 T, cylindrical (circular or elliptical cross-section) bore, whole body MR scanners operating at approximately 64 MHz with whole body coil excitation. ISO/TS 10974:2012 Withdrawn: Number of pages: 214 Price: NOK 2 140,00 (excl. VAT) NOK 2 675,00 (with VAT) Scope ISO (the International Organization for Standardization) is a worldwide federation of national standards bodies (ISO member bodies). The work of preparing International Standards PD ISO-TS 10974-2018. BSI Standards Publication WB11885_BSI_StandardCovs_2013_AW.indd 1 15/05/2013 1506 Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device PD ISO/TS 109742018National foreword This Published Document is the UK implementation of ISO/TS 109742018.