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
| File Size : | 1
file
, 2.9 MB |
| ISBN(s) : | 9780580916748 |
| Note : | This product is unavailable in Ukraine, Russia, Belarus |
| Number of Pages : | 78 |
| Product Code(s) : | 30330345, 30330345, 30330345 |
| Published : | 04/17/2018 |