(2016), 3: ASTM F2503-13 (2013), 4: ISO/TS 10974 (2018), 5: ASTM F2119-07 ( 2013), 6: ASTM. F2052-15 (2015), 7: ASTM F2213-17 (2017), 8: Azadarmaki et 

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Iso ts 10974

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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

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Iso ts 10974

Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device - ISO/TS 10974:2012

Iso ts 10974

For more information and personal contact ple ISO/TS 10974:2018 Published: Number of pages: 200 Price: NOK 665,00 (excl. VAT) NOK 831,25 (with VAT) Scope ISO/TS 10974:2012-05 Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device German title Anforderungen an Sicherheit und Kompatibilität der Magnetresonanztomographie für Patienten mit einem aktiven implantierbaren Medizinprodukt Publication date 2012-05 Original language English 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. •ISO TS 10974 (JWG): interactions between MRI scanner and implanted device •A horizontal standard attempting coverage of all active implants, but no requirements •ISO SC6 (responsible implant committee): responsible for implants and the safety of the implant patient ISO - ISO/CD 10974 - Assessment of the safety of magnetic resonance imaging for patients with an active implantable medical device. Skip to main content. Standards >. Benefits >.

Iso ts 10974

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. Technical specification ISO/TS 10974 describes test methods to assess possible malfunctions due to individual and combined magnetic fields.
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Iso ts 10974

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The draft was circulated for voting to the national bodies of both ISO and IEC. This second edition cancels and replaces the first edition (ISO/TS 10974:2012) which has been technically revised. Abstract. ISO/TS 10974:2012 is applicable to implantable parts of active implantable medical devices (AIMDs) intended to be used in patients who might undergo a magnetic resonance scan in 1,5T, cylindrical bore, whole body MR scanners for imaging the hydrogen nucleus. The tests that are specified in ISO/TS 10974:2012 are type tests intended to be carried out on samples of a device to characterize interactions with the magnetic and electromagnetic fields associated with an MR scanner.


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ISO/TS 10974:2012 is applicable to implantable parts of active implantable medical devices (AIMDs) intended to be used in patients who might undergo a magnetic resonance scan in 1,5T, cylindrical bore, whole body MR scanners for imaging the hydrogen nucleus. The tests that are specified in ISO/TS 10974:2012 are type tests intended to be carried out

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ISO/TS 10974:2018(E) Foreword ISO (the International Organization for Standardization) is a worldwide federation of national standards bodies (ISO member bodies). The work of preparing International Standards is normally carried out through ISO technical committees. Each member body interested in a subject for which a technical

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