
Medical electrical equipment Part 2-16: Particular requirements for the safety of haemodialysis, haemodiafiltration and haemofiltration equipment
出版:International Electrotechnical Committee

专家解读视频
Specifies the minimum safety requirements for single patient haemodialysis, haemodiafiltration and haemofiltration equipment. These devices are intended for use either by medical staff or under the supervision of medical expertise, including haemodialysis, haemodiafiltration and haemofiltration equipment operated by the patient.
ONORM OVE EN 60601-2-16:1998 - Identical
DIN EN 60601-2-16 (1999-02) - Identical
NBR IEC 60601-2-16:2003 - Identical
BS 5724-2.16:1998 - Equivalent
BS EN 60601-2-16:1998 - Equivalent
NEN EN IEC 60601-2-16:1998 - Identical
SN EN 60601-2-16:1998 - Identical
CEI EN 60601-2-16 Ed. 1 (1999) - Identical
UNE 20613-2-16:1992 - Identical
SS IEC 601-2-16 Ed. 1 (1991) - Similar
SS EN 60601-2-16:1998 - Identical
UNE EN 60601-2-16:1999 - Identical
AS/NZS 3200.2.16:1999 - Identical
PN EN 60601-2-16:2006 - Identical
CSA C22.2.60601.2.16:2001 (R2005) - Identical
I.S. EN 60601-2-16:1999 - Identical
HD 395.2.16:1988 - Similar
NF EN 60601-2-16:2002 - Identical
VDE 0750-2-16:1999 - Identical
BS 5724-2-2.16:1989 - Similar