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About This Item

 

Full Description

BS EN 61391-1:2006+A1:2017: A quality assessment system is vitally needed to provide an accurate and well-defined set of production-quality parameters for new or refurbished scanners or transducers in acceptance tests before their introduction to medical practice. It is important that products delivered by third-party sales groups, system-refurbishers and/or transducer manufacturers be carefully tested to be able to declare technical parameters of their products to be comparable to those of the new, originally manufactured systems. The methods used for quality assessment in medical applications are not certain and accurate enough to be used for such kinds of technical performance evaluation. PSF-mapping analysis gives reliable parameters suitable for this kind of tests. These parameters do not directly indicate the effectivity of a clinical diagnostic process, even though a close correlation between the assessed technical quality and success in the diagnostic process may be expected [40].


Cross References:
IEC 60050-802:2011
EN 62127-1 (IEC 62127-1:2007) AS
IEC 61685:2001
IEC 62127-1:2007
IEC 60050-801:1994
EN 61157:1994
IEC 60050-802
IEC TR 62781:2012
IEC 61391-2:2010
IEC TS 62791:2015
EN 61391-2 (IEC 61391-2:2010) AS
IEC 61828:2001
IEC TS 62736:2016
IEC 60854:1986
IEC TS 62558:2011
ISO 5725-1:1994
EN 62563-1 (IEC 62563-1:2009) AS
EN 61828 (IEC 61828:2001)
IEC 62563-1:2009
IEC 61390:1996
IEC 61157:1992


Incorporates the following:
Amendment, April 2018
 

Document History

  1. BS EN 61391-1:2006+A1:2017

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    Ultrasonics. Pulse-echo scanners-Techniques for calibrating spatial measurement systems and measurement of system point-spread function response

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  2. BS EN 61391-1:2006


    Ultrasonics. Pulse-echo scanners. Techniques for calibrating spatial measurement systems and measurement of system point-spread function response

    • Historical Version