Hivatkozási szám

MSZ EN 50527-2-2:2018

Dokumentumazonosító

168682

Cím

Eljárás az aktív beültethető orvostechnikai eszközökkel élő, elektromágneses tereknek kitett munkavállalók expozíciójának értékelésére. 2-2. rész: Egyedi értékelés beültethető kardioverter-defibrillátorokkal (ICD-kkel) élő munkavállalók esetén

Angol cím

Procedure for the assessment of the exposure to electromagnetic fields of workers bearing active implantable medical devices. Part 2-2: Specific assessment for workers with cardioverter defibrillators (ICDs)

Alkalmazási terület

This European Standard provides the procedure for the specific assessment required in EN 50527-1:2016, Annex A, for workers with implanted cardioverter defibrillators (ICDs) and Cardiac Resynchronization Therapy devices with associated defibrillation functions (CRT-D). Only devices of this type equipped with leads implanted transvenously are considered. It offers different approaches for doing the risk assessment. NOTE 1 If the worker has other Active Implantable Medical Devices (AIMDs) implanted additionally, they are assessed separately according to EN 50527–1 or other particular standards within the EN 50527 series. NOTE 2 The risks to patients due to interference with pacing functions associated with CRT-D devices are assessed using EN 50527–2-1. The purpose of the specific assessment is to determine the risk for workers with implanted ICDs and CRT-Ds arising from exposure to electromagnetic fields (EMF) at the workplace. The assessment includes the likelihood of clinically significant effects and takes account of both transient and long-term exposure within specific areas of the workplace. NOTE 3 This standard does not address risks from contact currents. The techniques described in the different approaches may also be used for the assessment of publicly accessible areas. The frequency range to be observed is from 0 Hz to 3 GHz. Above 3 GHz no interference with the devices within the scope of this Particular Standard is expected to occur when the exposure limits are not exceeded. NOTE 4 The rationale for limiting the observation range to 3 GHz can be found in ISO 14117:2012, Clause 5. NOTE 5 Further information concerning the functions of Pacemakers, CRT-D, and ICD devices can be found in Ellenbogen and Kaszala, 2014.

ICS

11.040.40 Sebészeti implantátumok, protézisek és ortézisek

17.240 Sugárzásmérések

Műszaki Bizottság

A szabvány nyelve

angol

Az érvényesség kezdete

2018-09-01

Forrás

idt EN 50527-2-2:2018

Előd

Utód

Módosítás

SZK-közlemények

Kapcsolódó európai jogszabály

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

A szabvány

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