
Medical electrical equipment Part 2-17: Particular requirements for the safety of automatically-controlled brachytherapy afterloading equipment
出版:International Electrotechnical Committee

专家解读视频
The use of afterloading equipment for brachytherapy purposes may expose patients to danger if the equipment fails to deliver the required dose to the patient, or if the equipment design does not satisfy standards of electrical and mechanical safety. The equipment may also cause danger to persons in the vicinity if the equipment itself fails to contain the radioactive source(s) adequately within the storage container(s) and/or if there are inadequacies in the design of the treatment room. This Particular Standard establishes requirements to be complied with by manufacturers in the design and construction of afterloading equipment for use in temporary brachytherapy procedures. Its purpose is to identify those features of design that are regarded, at the present time, as essential for the safe operation of such equipment. It places limits on the degradation of equipment performance beyond which it can be presumed that a fault condition exists and where an interlock then operates to return the radioactive source(s) to the storage container(s) and afterwards to prevent continued operation of the equipment.
BS EN 60601-2-17:2004 - Identical
DIN EN 60601-2-17 (2004-12) - Identical
NF EN 60601-2-17:2005 - Identical
UNE EN 60601-2-17:2005 - Identical
OVE/ONORM EN 60601-2-17:2005 - Identical
NEN EN IEC 60601-2-17:2004 - Identical
CSA C22.2.601.2.17:1994 (R1999) - Identical
CSA C22.2.60601.2.17:2004 (R2014) - Identical
PN EN 60601-2-17:2007 - Identical
CEI EN 60601-2-17 Ed. 2 (2006) - Identical
SN EN 60601-2-17:1996 - Identical
BS 5724-2.17:1990 - Identical
ONORM EN 60601-2-17:1998 - Identical
ONORM OVE EN 60601-2-17:1998 - Identical
NFC 74 210:1992 - Identical
JIS Z 4620:1999 - Identical
NEN 10601-2-17:1996 - Identical
SS EN 60601-2-17 Ed. 2 (2004) - Identical
VDE 0750-2-17:2004 - Identical
I.S. EN 60601-2-17:2004 - Identical