IEC/TR 62653:2012

Guidelines for the safe use of medical products in dialysis treatment IEC/TR 62653:2012

Publication date:   Sep 12, 2013

95.99   Withdrawal of Standard   Oct 20, 2020

General information

95.99   Withdrawal of Standard   Oct 20, 2020

IEC

ISO/TC 150/SC 2 Cardiovascular implants and extracorporeal systems

Technical Report

11.040.40   Implants for surgery, prosthetics and orthotics

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Scope

IEC/TR 62653:2012(E) which is a technical report, describes the technical requirements for use of equipment in haemodialysis, haemofiltration and haemodiafiltration. These principles should be complied with to ensure safe, permissible and proper application. The physician is responsible for the haemodialysis treatment prescription. However, the organization administering the treatment is responsible for all resources, structures and processes used in connection with the treatment. These responsibilities will not be described here. If applicable, the scope may be applicable to the use of the equipment in paediatrics, home haemodialysis, acute and sorbent dialysis systems. This technical report is not intended to be used as the basis of regulatory inspection or certification assessment activities.

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IEC/TR 62653:2012
95.99 Withdrawal of Standard
Oct 20, 2020




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