BS EN 60601-2-64:2015 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of LIGHT ION BEAM ME EQUIPMENT, hereafter referred to as ME EQUIPMENT, used for treatment of PATIENTS.

If a clause or subclause is specifically intended to be applicable to ME EQUIPMENT only, or to ME SYSTEMS only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME EQUIPMENT and to ME SYSTEMS, as relevant.

This particular standard, with the inclusion of TYPE TESTS and SITE TESTS, applies respectively to the manufacture and some installation aspects of LIGHT ION BEAM ME EQUIPMENT

• intended for RADIOTHERAPY in human medical practice, including those in which the selection and DISPLAY of operating parameters can be controlled automatically by PROGRAMMABLE ELECTRONIC SUBSYSTEMS (PESS),
• that, in NORMAL USE, deliver a RADIATION BEAM of LIGHT IONS having ENERGY PER NUCLEON in the range 10 MeV/n to 500 MeV/n,

and

• intended to be
  • for NORMAL USE, operated under the authority of appropriately licensed or QUALIFIED PERSONS by OPERATORS having the required skills for a particular medical application, for particular SPECIFIED clinical purposes maintained in accordance with the recommendations given in the INSTRUCTIONS FOR USE,
  • subject to regular quality assurance performance and calibration checks by a QUALIFIED PERSON.

Cross References:
IEC 60601-1-2:2014
EN 60601-1-2:2014
IEC 60601-1:2005
IEC 60601-1:2005/A1:2012
EN 60601-1:2006
EN 60601-1:2006/Corrigendum 1:2010
EN 60601-1:2006/A1:2013
EN 60601-1:2006/A1:2013/Corrigendum 1:2014
EN 60601-1:2006/A12:2014
IEC 60601-2-1:2009
IEC 60601-2-11:2013
EN 60601-2-11:2015
IEC/TR 60788:2004
IEC 61217:2011
EN 61217:2012
ISO/IEC 14165-321:2009
IEC 60601-2-68
EN 60601-2-68
93/42/EEC
ICRU Report 33:1980
ICRU Report 85a:2011


All current amendments available at time of purchase are included with the purchase of this document.