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EN 60601-2-16:1998

Medical electrical equipment - Part 2-16: Particular requirements for the safety of haemodialysis, haemodiafiltration and haemofiltration equipment EN 60601-2-16:1998

Publication date:   Mar 19, 2004

General information

99.60 Withdrawal effective   Apr 14, 2018

CENELEC

CLC/TC 62 Electrical equipment in medical practice

European Norm

11.040   Medical equipment | 11.040.20   Transfusion, infusion and injection equipment

Buying

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Scope

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.

Related legislation

Legislation related to this standard

93/42/EEC

Medical devices

Harmonized/Supporting
Legislation 93/42/EEC

Life cycle

PREVIOUSLY

WITHDRAWN
HD 395.2.16 S1:1989

NOW

WITHDRAWN
EN 60601-2-16:1998
99.60 Withdrawal effective
Apr 14, 2018

CORRIGENDA / AMENDMENTS

WITHDRAWN
EN 60601-2-16:1998/corrigendum Dec. 1999

REVISED BY

WITHDRAWN
EN 60601-2-16:2015