My employer designs and manufactures, among other things, component power
supplies for medical, IT, instrument, industrial, and other weird stuff. 

Unlike other safety-critical components such as X/Y caps, VDRs, switches,
connectors, etc; there are no 'accepted' safety standards for component power
supplies. No need to tell me about IEC61204, UL1310, UL1012, IEC61558, etc; as
these are 'boutique' standards. Each major product safety standard has some
specific requirements for power sources - of which most requirements overlap.
Other than an indicated conformity to Articles 600 or 725 of NEC, it is very
unusual to be able to drop in a component power supply from different sources
even when the ratings are identical.

Until there is an industry-standard component power supply product safety
standard that has been harmonized by all national codes, and is cited in the
Big Four (60950/60065/60335/60601), there will be no drop-in replacements
without re-test with an alternate construction amendment to your CB report.

Final note - I have recent experience where a CPS with a 60601 report, and
tested for patient contact, was installed in ITE. The box could no longer pass
all safety requirements for a C.O. device. This has been discussed in previous
PSES threads - a medical power supply is not necessarily 'safe' in a consumer
or ITE box.

Brian 

 > -----Original Message-----
 > From: [email protected] [mailto:[email protected]]On Behalf Of Amund
 > Westin
 > Sent: Wednesday, September 15, 2010 12:19 AM
 > To: [email protected]
 > Subject: SV: [PSES] IEC 60950-1 vs IEC 60601-1
 > 
 > The end product is an ITE (DVB) and in the previous models, 
 > we have made use
 > of an open frame AC/DC power supply unit. This PSU had CB certificate
 > according to IEC60950-1. Then we went to a third party body 
 > for testing the
 > complete unit according to IEC60950-1. Since we had a CB 
 > certificate, the
 > scope of work for testing the ITE was limited a lot, since 
 > no testing /
 > examination on the PSU itself was necessary.
 > 
 > Now, we want to change PSU to another open frame AC/DC power 
 > supply unit.
 > This PSU has a CB cert acc to IEC 60601-1, while the end 
 > product still shall
 > conform according to IEC60950-1. 
 > 
 > Since the new PSU shall be placed inside the ITE, some 
 > safety test and
 > evaluations must be done. 
 > But we would also assume that a 601-1 PSU should be more 
 > "safe" than an
 > 950-1 PSU, seen from an application point of view.
 > 
 > We accept that some safety testing must be done on the end 
 > product. But we
 > find it a bit strange if the introduction of this medical 
 > PSU involves more
 > testing than if we had made use of a 950-1 PSU.
 > 
 > #Amund
 >  
 > 
 > -----Opprinnelig melding-----
 > Fra: Brian O'Connell [mailto:[email protected]] 
 > Sendt: 14. september 2010 18:56
 > Til: [email protected]
 > Emne: Re: [PSES] IEC 60950-1 vs IEC 60601-1
 > 
 > WARNING - Fractious dichotomous isochroous nondeterministic 
 > reply follows.
 > 
 > I am not certain of Mr. Westin's use of "PSU". IEC60950-1 
 > has no definition
 > for the phrase 'power supply unit', and contextual meaning is not
 > consistent. IEC60601-1 uses the phrase 'power supply unit' only when
 > referring to a separate external power source.
 > 
 > For a COMPONENT power supply, where the final determination 
 > is the end-use
 > installation - the 'PSU' CB report can use a TRF based on 
 > almost any product
 > safety standard that would scope a 'PSU'.
 > 
 > For a power supply that has been assessed as an end-product, neither
 > standard provides complete coverage for the requirements of 
 > the other for
 > many uses, and for some uses either standard could provide 
 > coverage for a
 > superset of the requirements. Anyone wanna see a De Morgan 
 > reduction of that
 > logic ?
 > 
 > The coming (????) of the UL/EN/IEC62368-1 standard may 
 > provide an unintended
 > formal method to 'bridge' various requirements for component 
 > power supplies.
 > 
 > Most I.T. CB reports for component power supplies require 
 > the repeat of some
 > Type Tests in the end-use installation. So for a medical 
 > 'PSU', the pudding
 > would not get cooked until it was subject to tests in your I.T. box.
 > Conversely, the 3d edition of 60601-1 specifically addresses 
 > the use of I.T.
 > component power supplies for some medical equipment.
 > 
 > The CB report could be considered valid; or not.
 > Additional tests could be required; or not.
 > 
 > Non-related Note: the '#' at the signature threw some 
 > interesting errors for
 > my auto-mail program - thanks for the programmatic work-out.
 > 
 > Brian 
 > 
 >  > -----Original Message-----
 >  > From: [email protected] [mailto:[email protected]]On 
 > Behalf Of Amund
 >  > Westin
 >  > Sent: Tuesday, September 14, 2010 1:05 AM
 >  > To: [email protected]
 >  > Subject: IEC 60950-1 vs IEC 60601-1
 >  > 
 >  > Is it possible to make use of a CB certificated (IEC 
 >  > 60601-1) PSU, into a
 >  > ITE which shall be approved according to IEC60950-1?
 >  > 
 >  > Well, I assume that's OK, but should we expect additional 
 >  > tests on the PSU /
 >  > ITE since it's not CB acc to IEC60950-1?
 >  > 
 >  > Thanks.
 >  > #Amund

-
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