Hivatkozási szám

MSZ EN 50527-1:2017

Dokumentumazonosító

165010

Cím

Eljárás az aktív beültethető orvostechnikai eszközökkel élő, elektromágneses tereknek kitett dolgozók expozíciójának értékelésére. 1. rész: Általános előírások

Angol cím

Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices. Part 1: General

Alkalmazási terület

This European Standard provides a procedure to assess the risk to workers bearing one or more active implantable medical devices from exposure to electric, magnetic and electromagnetic fields at a workplace. It describes how a general risk assessment should be performed and determines whether it is necessary to carry out a detailed risk assessment. NOTE 1 This European Standard does not cover indirect effects caused by non active implants. NOTE 2 The risk of human exposure to EMF considered is only due to malfunctioning of AIMD. Possibilities of AIMD contribution to the risk, e.g. local modification of the distribution of EMF produced by external source or production of own EMF, are covered by the respective product standards for the AIMD. Based on specific workplace standards it can be determined whether preventive measures/actions need to be taken to comply with the provisions of Directive 2013/35/EU. The work situation covered is considered to be under normal working conditions including normal operation, maintenance, cleaning and other situations being part of the normal work. The frequencies covered are from 0 Hz to 300 GHz. The European Parliament and Council Directive 2013/35/EU will be transposed into national legislation in all the EU member countries. It is recommended that users of this standard consult the national legislation related to this transposition in order to identify the national regulations and requirements. These national regulations and requirements may have additional requirements that are not covered by this standard and take precedence. NOTE 3 Performance requirements with respect to active implantable medical devices are excluded from the Scope of this standard. These are defined in the relevant particular standards for active implantable medical devices. The risk assessment described in this standard is only required if an AIMD-Employee is present. Active Implantable Medical Devices (AIMDs) are regulated by Directive 90/385/EEC and the amendments to it. NOTE 4 Product standards EN 45502–1 and of the EN 45502–2-X series describe the product requirements for different kinds of AIMDs. Different kinds of AIMDs are e.g. pacemaker (EN 45502–2–1), implantable cardioverter defibrillators (EN 45502–2–2), cochlear implants (EN 45502–2–3), implantable neurostimulators (ISO 14708-3), implantable infusion pumps (ISO 14708-4). In situations where the risk assessment following this standard does not lead to a conclusion, complementary provisions for the assessment of workers exposure for different kinds of AIMDs are given in particular standards for these specific AIMDs (see Figure 1). Ábra

ICS

11.040.40 Sebészeti implantátumok, protézisek és ortézisek

13.100 Munkavédelem. Ipari egészségügy

13.280 Sugárvédelem

Műszaki Bizottság

A szabvány nyelve

angol

Az érvényesség kezdete

2017-05-01

Forrás

idt EN 50527-1:2016

Előd

MSZ EN 50527-1:2010

Utód

Módosítás

Kiegészítő információk

SZK-közlemények

Kapcsolódó európai jogszabály

2004/40/EK (EMF04); 2013/35/EU (EMF13)

A szabvány

kapható formátuma

Papír ,
PDF (letöltés) (a fájl mérete: 913025) ,

oldalszáma

35 oldal; Q kategória

ára

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