Pat:
61000-3-2 is a horizontal standard and it applies to all products unless
specifically excluded by 61000-3-2.  The criteria is defined by CENELEC and
it is not necessarily specified by the individual product standards.  This
is why it is so important to watch basic and horizontal standards even
though they may not called out in the product standards. These
cross-the-board standards are sleepers and can effect manufacturer's through
the back door.  

Industry has decided to fight 61000-3-2 in the IEC and try to achieve
realistic requirements.  The US national committee has just released a
position paper on harmonics requirements.  If anyone needs a copy I can post
it on this net.
Dave George
Unisys

-----Original Message-----
From: plaw...@west.net [mailto:plaw...@west.net]
Sent: Thursday, June 17, 1999 7:55 PM
To: emc-p...@majordomo.ieee.org
Subject: Medical Device Directive, IEC 601-1-2, and IEC 1000-3-2



I was asked the following question, and wasn't sure about the answer:

1) A manufacturer can claim his system complies with the Medical Device
Directive by testing to EN 60601-1-2:1993.

2) EN 60601-1-2:1993 does not have any requirements to test to IEC 1000-3-2.

3) Does that mean that the harmonic standard does not apply to this system
when
it becomes mandatory in 2001?


I realize the Second Edition of IEC60601-1-2 is just around the corner, and
that edition _does_ call out the harmonic test.  However, I've been told
that
it may not take effect until 2003.
--
Patrick Lawler
plaw...@west.net

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