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SRPS EN ISO 14708-3:2022

Implants for surgery - Active implantable medical devices - Part 3: Implantable neurostimulators (ISO 14708-3:2017)

Dec 30, 2022

General information

60.60     Dec 30, 2022

ISS

Z076

European Norm

11.040.40  

English  

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Scope

ISO 14708-3:2017 is applicable to active implantable medical devices intended for electrical stimulation of the central or peripheral nervous system.
The tests that are specified in this document are type tests and are to be carried out on a sample of a device to assess device behavioural responses, and are not intended to be used for the routine testing of manufactured products.

Related directives

NOTE: If the word "harmonized" (marked in green) is not found in the field with the name of the directive, it means that the European standard is not cited in the OJEU.

2017/745

Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC

Life cycle

NOW

PUBLISHED
SRPS EN ISO 14708-3:2022
60.60 Standard published
Dec 30, 2022

Related project

Adopted from EN ISO 14708-3:2022

Adopted from ISO 14708-3:2017