درباره ما
CSA CAN/CSA-C22.2 NO. 60601-2-16-09
Medical electrical equipment — Part 2-16: Particular requirements for basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment - Third Edition
Organization:
CSA - CSA Group
Year: 2009
Abstract: Addition:
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of HAEMODIALYSIS, HAEMODIAFILTRATION and HAEMOFILTRATION EQUIPMENT, hereafter referred to as HAEMODIALYSIS EQUIPMENT.
This International standard does not take into consideration the DIALYSING FLUID control system of HAEMODIALYSIS EQUIPMENT using regeneration of DIALYSING FLUID and CENTRAL DELIVERY SYSTEMS. It does however take into consideration the specific safety requirements of such HAEMODIALYSIS EQUIPMENT concerning electrical safety and PATIENT safety.
This International standard specifies the minimum safety requirements for HAEMODIALYSIS EQUIPMENT. These devices are intended for use either by medical staff or for use by the PATIENT or other trained personnel under the supervision of medical expertise.
This International standard includes all ME EQUIPMENT that is intended to deliver a HAEMODIALYSIS, HAEMODIAFILTRATION and HAEMOFILTRATION treatment to a PATIENT suffering from kidney failure.
The particular requirements in this International standard do not apply to:
– EXTRACORPOREAL CIRCUITS;
– DIALYSERS;
– DIALYSING FLUID CONCENTRATES;
– water treatment equipment;
– equipment used to perform PERITONEAL DIALYSIS (see IEC 60601-2-39).
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.
HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this standard are not covered by specific requirements in this standard except in 7.2.13 and 8.4.1 of IEC 60601-1.
NOTE See also 4.2 of IEC 60601-1:2005.
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of HAEMODIALYSIS, HAEMODIAFILTRATION and HAEMOFILTRATION EQUIPMENT, hereafter referred to as HAEMODIALYSIS EQUIPMENT.
This International standard does not take into consideration the DIALYSING FLUID control system of HAEMODIALYSIS EQUIPMENT using regeneration of DIALYSING FLUID and CENTRAL DELIVERY SYSTEMS. It does however take into consideration the specific safety requirements of such HAEMODIALYSIS EQUIPMENT concerning electrical safety and PATIENT safety.
This International standard specifies the minimum safety requirements for HAEMODIALYSIS EQUIPMENT. These devices are intended for use either by medical staff or for use by the PATIENT or other trained personnel under the supervision of medical expertise.
This International standard includes all ME EQUIPMENT that is intended to deliver a HAEMODIALYSIS, HAEMODIAFILTRATION and HAEMOFILTRATION treatment to a PATIENT suffering from kidney failure.
The particular requirements in this International standard do not apply to:
– EXTRACORPOREAL CIRCUITS;
– DIALYSERS;
– DIALYSING FLUID CONCENTRATES;
– water treatment equipment;
– equipment used to perform PERITONEAL DIALYSIS (see IEC 60601-2-39).
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.
HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this standard are not covered by specific requirements in this standard except in 7.2.13 and 8.4.1 of IEC 60601-1.
NOTE See also 4.2 of IEC 60601-1:2005.
Collections
:
-
Statistics
CSA CAN/CSA-C22.2 NO. 60601-2-16-09
Show full item record
| contributor author | CSA - CSA Group | |
| date accessioned | 2017-09-04T18:47:35Z | |
| date available | 2017-09-04T18:47:35Z | |
| date copyright | 2009.11.01 | |
| date issued | 2009 | |
| identifier other | KMJKPCAAAAAAAAAA.pdf | |
| identifier uri | http://yse.yabesh.ir/std;query=autho1626AF679D40527361598F1ED52F014A/handle/yse/228770 | |
| description abstract | Addition: This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of HAEMODIALYSIS, HAEMODIAFILTRATION and HAEMOFILTRATION EQUIPMENT, hereafter referred to as HAEMODIALYSIS EQUIPMENT. This International standard does not take into consideration the DIALYSING FLUID control system of HAEMODIALYSIS EQUIPMENT using regeneration of DIALYSING FLUID and CENTRAL DELIVERY SYSTEMS. It does however take into consideration the specific safety requirements of such HAEMODIALYSIS EQUIPMENT concerning electrical safety and PATIENT safety. This International standard specifies the minimum safety requirements for HAEMODIALYSIS EQUIPMENT. These devices are intended for use either by medical staff or for use by the PATIENT or other trained personnel under the supervision of medical expertise. This International standard includes all ME EQUIPMENT that is intended to deliver a HAEMODIALYSIS, HAEMODIAFILTRATION and HAEMOFILTRATION treatment to a PATIENT suffering from kidney failure. The particular requirements in this International standard do not apply to: – EXTRACORPOREAL CIRCUITS; – DIALYSERS; – DIALYSING FLUID CONCENTRATES; – water treatment equipment; – equipment used to perform PERITONEAL DIALYSIS (see IEC 60601-2-39). 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. HAZARDS inherent in the intended physiological function of ME EQUIPMENT or ME SYSTEMS within the scope of this standard are not covered by specific requirements in this standard except in 7.2.13 and 8.4.1 of IEC 60601-1. NOTE See also 4.2 of IEC 60601-1:2005. | |
| language | English | |
| title | CSA CAN/CSA-C22.2 NO. 60601-2-16-09 | num |
| title | Medical electrical equipment — Part 2-16: Particular requirements for basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment - Third Edition | en |
| type | standard | |
| page | 70 | |
| status | Active | |
| tree | CSA - CSA Group:;2009 | |
| contenttype | fulltext |