Thanks Bernd.  Does it sound like it also covered magnetic fields from fixed
magnets?

 

Dan

 

 

From: Dürrer Bernd [mailto:bernd.duer...@wilo.com] 
Sent: Tuesday, November 08, 2022 4:19 AM
To: EMC-PSTC@LISTSERV.IEEE.ORG
Subject: [PSES] AW: [PSES] Magnetic fields, human exposure standards, and
pacemakers

 

Hello Dan,

 

on
https://www.bfarm.de/DE/Medizinprodukte/Aufgaben/Risikobewertung-und-Forschu
ng/Wissenschaftliche-Aufarbeitung/EMV-Studie_Herzschrittmacher.html you may
find a press release from the German Bundesinstitut für Arzneimittel und
Medizinprodukte (BfArM; Federal Institute for Drugs and Medical Devices) on
a “Study on the immunity of implantable pacemakers of the Institut für
Rundfunktechnik GmbH, Munich”. In this study, the EMC immunity of 274
pacemaker devices was tested according to European standard EN 45502-2-1 (
<https://standards.cencenelec.eu/dyn/www/f?p=CENELEC:110:::::FSP_PROJECT,FSP
_ORG_ID:20265,2401823&cs=1B2A778F33C4A9FE02D07532CE3EAC191> CENELEC -
CEN/CLC/JTC 16 (cencenelec.eu)) and American standard ANSI/AAMI PC69 (
<https://webstore.ansi.org/Standards/AAMI/ANSIAAMIPC692007PC69> ANSI/AAMI
PC69:2007 (ANSI/AAMI PC 69:2007) - Active implantable medical devices -
Electromagnetic compatibility - EMC test protocols for implantable cardiac
pacemakers and implantable cardioverter defibrillators (Includes Erratum)).
The press release is in German only, but here is a translation of the
summary:

 

“Through the use of a standard-compliant measurement setup and the automated
measurements of PM, which in their model diversity represent about 95% of
the market for active pacemakers as of 2004, the study offers the most
comprehensive overview to date of device behavior under the influence of
electromagnetic interference at different frequencies. In the area of mobile
radio frequencies, no failures were observed in the study, but often in the
frequency range below 450 MHz. Should electromagnetic interference occur in
practice, the device would automatically be switched to safe mode (backup
mode), where further operation is possible.

 

In theBfArM's reporting system, there is no accumulation of pacemaker events
due to EMC influences, and the BfArM has not reported any individual cases
of high error severity that show a fatal pacemaker failure caused by
interference. An event that comes into question for this, such as the
coincidence of an electromagnetic disturbance and the stimulation in the
vulnerable phase, is theoretically possible, but unlikely and this justifies
the very low statistical relevance of such exceptional cases from the point
of view of the BfArM.”

 

With respect to warnings in the instructions, the press release contains the
following statement:

 

“Many instructions for use contain not only an indication of the risks of
electromagnetic interference, but also a list of sources of interference
with appropriate warnings for the patient. If there is not even a general
indication of the possibility of interference by external electromagnetic
fields, it is necessary from the point of view of the BfArM to include a
corresponding warning in the device description in accordance with Annex 2.4
of AIMD 90/385/EEC.”

 

Kind regards,

 

Bernd

 

 

Von: Chas Grasso <charles.gra...@dish.com <mailto:charles.gra...@dish.com> >

Gesendet: Montag, 7. November 2022 16:16
An: EMC-PSTC@LISTSERV.IEEE.ORG <mailto:EMC-PSTC@LISTSERV.IEEE.ORG> 
Betreff: Re: [PSES] Magnetic fields, human exposure standards, and
pacemakers

 

Hello Dan, 

Dont you think that (irrespective of the warning ) the magnet on the DC cord
is *much* weaker than a magnet used to penetrate through the thickness of
the human body and then trigger the reed switches? My first thought is that
the warning is there as a CYA? Perhaps?

 

On Sun, Nov 6, 2022 at 2:06 PM Dan Roman
<00000d75e04ed751-dmarc-requ...@listserv.ieee.org
<mailto:00000d75e04ed751-dmarc-requ...@listserv.ieee.org> > wrote:

 This message originated outside of DISH and was sent by:
00000d75e04ed751-dmarc-requ...@listserv.ieee.org
<mailto:00000d75e04ed751-dmarc-requ...@listserv.ieee.org>  

 

  _____  

Thank you everyone for the responses.  Contacting the customer support
number gets you to someone who basically reads back what is on the website
and the user manual, so it was not particularly helpful when trying to get
to the specifics.

 

In a roundabout way through a friend of a friend I managed to arrange a
phone call with someone from Boston Scientific that had technical
engineering knowledge and could answer my questions.  The device in question
is a pacemaker/defibrillator.  It happens to be MRI compatible but I didn’t
get into what that means with respect to magnetic fields, I think it
probably has a lot to do with not getting ripped out of your chest if you
get an MRI.

 

Anyway, it has two sets of reed switches embedded in it.  One reed switch
will react to a lower level magnet placed over it and that puts it into a
fixed pacing mode.  This is used for diagnosing in the doctor’s office.  The
magnet in a fitness tracker is not likely to be strong enough or to get
close enough to turn on the fixed pacing mode during normal wear, but they
still will tell you not to wear it to bed in case you contort in such a way
when sleeping to cause an issue.

 

The second reed switch reacts only to a much stronger magnetic field and
this is used to disable the defibrillator if you go in for an operation.
The anesthesiologist will apply a strong magnet over the device to disable
it for the duration of the operation.  Makes sense that as that is easier
than connecting up a programming device to disable it and then re-enable it
and it can be easily turned off in an emergency situation with no need for a
make/model specific programming set.

 

So the relative is going to keep the fitness tracker and not wear it to bed
(most of the time).  They lose the sleep tracking but that is not of as much
interest to them and they don’t have it when sleeping every few days to
charge it overnight anyway.

 

Not sure if all devices work the same way but sounds like for simplification
reasons this might be a standardized practice to make surgeon’s and other
health care work easier.

 

I should have asked about how “MRI compatible” works!  Now I’m curious.

 

Dan

 

 

From: MIKE SHERMAN [mailto:msherma...@comcast.net
<mailto:msherma...@comcast.net> ] 
Sent: Thursday, November 03, 2022 8:52 PM
To: EMC-PSTC@LISTSERV.IEEE.ORG <mailto:EMC-PSTC@LISTSERV.IEEE.ORG> 
Subject: Re: [PSES] Magnetic fields, human exposure standards, and
pacemakers

 

Dan -- 

 

I'd suggest that you have your relative call Support at the pacemaker/defib
manufacturer. On a slightly different project, I found a lot of on-line
information about device immunity, and I think we even called Support and
got additional clarifying information. Go to the source!

Mike Sherman 

Sherman PSC LLC 

Product Safety and Compliance Consulting 

On 11/03/2022 11:32 AM Dan Roman
<00000d75e04ed751-dmarc-requ...@listserv.ieee.org
<mailto:00000d75e04ed751-dmarc-requ...@listserv.ieee.org> > wrote: 

 

 

Hello list!

 

I have a relative with an implanted pacemaker/defibrillator who recently got
a fitness tracker that has a magnet for attachment/alignment of the charging
cord.  There are warnings in the user manual advising against people with
pacemakers using this product because of the magnets, which I assume are
fairly strong rare earth types.  I looked up the DoC for the tracker and the
EM field human exposure standards EN 50663 and EN 62479 are listed on the
DoC.  My question is do these standards and the similar IEC 62233 give a
reasonable assurance that a pacemaker would not be interfered with or are
these standards purely concerned with biological effects on the human body
only?  I would expect the pacemaker to be immune to a certain extent if it
is FDA listed and complies with IEC 60601-1-2.  I don’t know the model
number of their device but I would expect them all to be similar.  Do they
need to send back their fitness tracker?  Or is the warning just thrown in
because the lawyers wanted it?

 

Although products I work on need to meet these types of standards, I don’t
have much familiarity with these exposure standards because my products have
never failed

 

Regards,

 

Dan

 

______________________________________________________
Dan Roman, N.C.E.

Senior Member

IEEE Product Safety Engineering Society

mailto:dan.ro...@ieee.org



 

 

 

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-- 

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 (c) 303-204-2974

(w) 303-706-5467

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