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Standard Detayı
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TÜRK STANDARDI
(Direktif :90/385/EEC,93/42/EEC)
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TS No :
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TS EN 60601-1-6
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Kabul Tarihi :
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13.07.2010
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Hazırlık Grubu :
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Teknik Kurul |
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Doküman Tipi :
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Yürürlük Durumu :
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U (Yürürlükteki Standard/Standard) |
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Başlık :
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Elektrikli tıbbi donanım - Bölüm 1-6: Temel güvenlik ve gerekli performans için genel kurallar - Yardımcı standard: Kullanım kolaylığı |
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Başlık (İng) :
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Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability |
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Kapsam :
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Kapsam (İng) :
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IEC 60601-1-6:2010 specifies a process for a manufacturer to analyse, specify, design, verify and validate usability, as it relates to basic safety and essential performance of medical electrical equipment. This usability engineering process assesses and mitigates risks caused by usability problems associated with correct use and use errors, i.e., normal use. It can be used to identify but does not assess or mitigate risks associated with abnormal use. If the usability engineering process detailed in this collateral standard has been complied with and the acceptance criteria documented in the usability validation plan have been met (see 5.9 of IEC 62366:2007), then the residual risks, as defined in ISO 14971, associated with usability of me equipment are presumed to be acceptable, unless there is objective evidence to the contrary (see 4.1.2 of IEC 62366:2007). The object of this collateral standard is to specify general requirements that are in addition to those of the general standard and to serve as the basis for particular standards. This document cancels and replaces the second edition of IEC 60601-1-6 which has been technically revised. It was revised to align with the usability engineering process in IEC 62366. To allow for equipment manufacturers and testing organizations to make products and to equip themselves for conducting revised tests in accordance with this third edition, it is recommended by SC 62A that the content of this document not be adopted for mandatory implementation earlier than 3 years from the date of publication for equipment newly designed and not earlier than 5 years from the date of publication for equipment already in production. |
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Yerini Aldığı :
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TS EN 60601-1-6 :2008; TS EN 60601-1-6/AC :2011; |
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Tadil Eden :
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TS EN 60601-1-6/A1 :2015; TS EN 60601-1-6/A2 :2021; |
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Yararlanılan Kaynak :
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EN 60601-1-6:2010 |
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Uluslararası Karşılıklar :
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EN 60601-1-6-EQV |
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ICS Kodu :
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11.040 Tıbbi Ekipman; 11.040.01 Tıbbi Ekipman (Genel) |
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Cen/Cenelec :
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CENELEC/IEC |
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Dili :
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en |
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Renk Durumu :
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Siyah-Beyaz |
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Uygulama Durumu :
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Yürürlükte |
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Sayfa Sayısı :
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59 |
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Fiyatı :
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94,00 EURO (3.258,95 TL + %10 Kdv) |
| Çakışan Standart Varsa İptal Tarihi (DOW) | - |
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