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Publication details

Publication CODE Title
NBN EN IEC 60601-2-16:2019 (2019-05) MEDICAL ELECTRICAL EQUIPMENT - PART 2-16: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF HAEMODIALYSIS, HAEMODIAFILTRATION AND HAEMOFILTRATION EQUIPMENT
 
Price Excl. VAT Total number of pages, tables and drawings
25.00 € 3.
Description
NEW!IEC 60601-2-16:2018 is available as IEC 60601-2-16:2018 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition.

IEC 60601-2-16:2018 applies to the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment. IEC 60601-2-16:2018 does not take into consideration the dialysis fluid control system of Haemodialysis equipment using regeneration of dialysis 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. IEC 60601-2-16:2018 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. IEC 60601-2-16:2018 includes all electromedical equipment that is intended to deliver a haemodialysis, haemodiafiltration and haemofiltration treatment to a patient suffering from kidney failure. This fifth edition cancels and replaces the fourth edition of IEC 60601-2-16, published in 2012. This edition includes the following significant technical changes with respect to the previous edition: a) update of references to IEC 60601-1:2005 and IEC 60601-1:2005/AMD1:2012, of references and requirements to IEC 60601-1-2:2014, of references to IEC 60601-1-6:2010 and IEC 60601-1-6:2010/AMD1:2013, of references and requirements to IEC 60601-1-8:2006 and IEC 60601-1-8:2006/AMD1:2012, of references to IEC 60601-1-9:2007 and IEC 60601-1-9:2007/AMD1:2013, of references to IEC 60601-1-10:2007 and IEC 60601-1-10:2007/AMD1:2013 and of references to IEC 60601-1-11:2015; b) widening of the scope; c) editorial improvements; d) addition of requirements for anticoagulant delivery means; e) other few small technical changes.  
Class  C
Available files
ATTENTION: Belgian registered standards (NBN EN or NBN HD) are generally only available in English or French. Only the cover page is translated and the document itself is in English or in French.

Very important notice: 98% of the text of the NBN EN 55XXX, NBN EN 6XXXX comes from the IEC text which is NOT included. This text can be ordered here: IEC 60601-2-16:2018. For the series NBN EN 50XXX, the standards are however complete.

DE version
FR version
EN version
Status
Status Registered trilingual Belgian standard EN or FR or DE
Situation Currently active
Replaces  NBN EN 60601-2-16:2015
Origin
Committee TC 62/SC 62D
ELECTROMEDICAL EQUIPMENT
Responsible De heer VAN HECKE Luk
Approval
BEC Approval 2018-05-25
NBN Approval 2019-06-26
ICS-Code (International Standards Classification) 11.040.20 , 11.040.25
NBN Status New
Date of ratification (d.o.r.) 2018-05-25
Date of availability (d.a.v.) 2019-05-24
Date of announcement (d.o.a.) 2019-08-24
Date of publication (d.o.p.) 2019-11-24
Date of withdrawal former edition (d.o.w.) 2022-05-24
Correspondences with international standards
Relation International standard Date
is identical to EN IEC 60601-2-16:2019 2019-05-24
is identical to IEC 60601-2-16:2018 2018-04-20
Relations to belgian/foreign publications
Type Origin Code Date
Standard Belgium EN 61672-1
Standard Belgium EN ISO 3744
Standard Belgium NBN EN 60601-1-10:2008
Standard Belgium NBN EN 60601-1-10:2008/A1:2015
Standard Belgium NBN EN 60601-1-11:2015
Standard Belgium NBN EN 60601-1-2:2015
Standard Belgium NBN EN 60601-1-6:2010
Standard Belgium NBN EN 60601-1-6:2010/A1:2015
Standard Belgium NBN EN 60601-1-8:2007
Standard Belgium NBN EN 60601-1-8:2007/A1:2013