As I read EN 61326, it allows the manufacturer to specify the performance
criteria for each test.  The standard only requires that equipment shall not
become dangerous or unsafe as a result of the application of the tests.  Table
2 is only an example of evaluation of immunity test results.  The note states
“…performance criteria B and/or C may be accepted provided that both the
specification and the test report highlight such deviation(s) for the relevant
combination(s) of function and test.”

 

The standard does require that the deviations be listed in the specifications
in addition to the test report.  If the published specifications do not
describe the deviations, the manufacturer may be considered in noncompliance
with the standard.  If they have declared compliance via the standard, this
could be an issue.  If the manufacturer has chosen not to use the standards
route but claims compliance with the essential requirements of the directive,
you may have an argument if the peripheral is not suitable for its intended
use because of the deviation.

 

I agree with David Spencer; you are the customer and the vendor needs to meet
your requirements if they want you to buy their products.

 

Ted Eckert

Compliance Engineer

Microsoft Corporation

ted.eck...@microsoft.com

 

The opinions expressed are my own and do not necessarily reflect those of my
employer.

 

From: Kunde, Brian [mailto:brian_ku...@lecotc.com] 
Sent: Wednesday, November 05, 2008 9:59 AM
To: EMC-PSTC@LISTSERV.IEEE.ORG
Subject: Deviation of Performance Criteria

 

Greetings Compliance Experts.

 

Something disturbing came across my desk today I thought I would get your
opinion on it.

 

On a CE marked peripheral we buy/sell as part of our laboratory equipment
system, failed several immunity tests when we tested it as part of our system.
 When we notified the peripheral's manufacturer of the problem (yes, I'm being
purposely vague) they said the failures were ok and sent us a "Certificate of
Compliance" by a very very well know compliance lab with the following
statement:

 

Snip

 

EMC Immunity:

EN 61326-1:1997/A1:1998/A2:2001 EMC requirements for Electrical equipment for
measurement, control, and laboratory use.

- General Use for the following test with deviation of performance criteria to
Criteria "C" instead of "B".

EN 61000-4-2

EN 61000-4-3

EN 61000-4-4

 

Unsnip

 

 

The peripheral manufacture said the EMC test lab told them they can put the CE
marking on their product as long as they included the above deviation
statement in their documentation and DOC.  

 

Is this true or was there some kind of miscommunication between the test lab
and the peripheral manufacturer?  

 

With this line of thinking, our test lab will not have to fail anything in the
future; just pass it with a deviation in the requirements. (just kidding).

 

Thanks to all for your opinion.

 

The Other Brian

 

_________________________ 

LECO Corporation Notice: This communication may contain confidential
information intended for the named recipient(s) only. If you received this by
mistake, please destroy it and notify us of the error. Thank you. 

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Instructions: http://listserv.ieee.org/request/user-guide.html 

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