[PSES] Global EMC (Montreal) - Free seminar and open house - June 18

2013-06-13 Thread S Drysdale
Dear Group members,

In collaboration with CLD de Laval http://www.cldlaval.com and Laval
Technopole http://www.lavaltechnopole.com/ we wish to extend  invite to
attend our free bilingual seminar.  This can be followed by a tour of our
facility during our open house.

For details see the below:

http://tinyurl.com/GEMCLaval-June2013-Englishhttp://www.linkedin.com/share?viewLink=sid=s5749961350818328580url=http%3A%2F%2Ftinyurl%2Ecom%2FGEMCLaval-June2013-Englishurlhash=wzSSpk=profile_v2_activitypp=1poster=545241uid=5749961379150852096trk=NUS_UNIU_SHARE-title

Best Regards,

Scott Drysdale

Global EMC (Laval)

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[PSES] Pointer please.

2013-06-13 Thread McInturff, Gary
Where in the safety directives are the instructions for spare parts or service 
parts. We manufacture a device for an end customer but don't do the safety 
approvals - we are just designated as a factory. I haven't seen any activity in 
getting this device approved under the new edition of the standard and am 
concerned that it has fallen through the cracks by the customer.
I don't believe it's a current production system but they are maintaining the 
systems already in the field, meaning that this are service parts I believe, 
but I don't know exactly what allows them to continue importing them into 
Europe.

The real issue is that some of the plastic that had been used in the past isn't 
going to be available but it is described as a critical component in the safety 
files by manufacturers name. model type. We can replace the material with the 
same flame rating but the raw material is from a different supplier. Even if 
spare parts are allowed for a system with an out of date harmonized safety 
standard I don't think one can just change the components without some 
activity, but exactly what and how, add some notes to the technical file?

I've tried discussing the issue with the customer but can't get through the 
purchasers to the compliance people, to insure that this isn't just slipping 
through the cracks.




Esterline Interface Technologies

Featuring
ADVANCED INPUT, GAMESMAN, LRE MEDICAL, and MEMTRON  products

600 W. Wilbur Avenue
Coeur d'Alene, ID  83815-9496
Toll Free: 800-444-5923 X1XXX
Tel:  (208) 635-8
Fax: (208) 635-8

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Re: [PSES] Pointer please.

2013-06-13 Thread Crane, Lauren
Gary
AFIK none of the CE marking directives address replacement parts explicitly 
(with a couple exceptions). Several of the directives have established in their 
guidance materials that the directives apply only to so-called finished 
products - which can be loosely defined (sometimes just by context) as a 
product intended for direct use by and end user. The machinery directive 
guidance makes clear the MD does not apply to 'components'. The new RoHS FAQ 
makes clear RoHS2 (CE, and maybe safety) does not apply to replacement parts 
for out of scope equipment, but watch out because RoHS2 does name spare 
parts. The old WEEE (not CE, and not safety) had a nice turn of phrase that 
exempted components incorporated in other equipment.  The many ERP regulations 
(CE, but not safety) scope as 'XYZ on their own and incorporated in other 
products' - which probably brings in replacement parts that are themselves XYZ. 
REACH (not CE, maybe safety) doesn't care about products and spare parts and 
only sees articles, so everything is in scope.

It's a real mixed bag. I've heard the old Blue Guide is under revision. Maybe 
they will help clarify your question in it.

Regards,
Lauren Crane
KLA-Tencor

From: McInturff, Gary [mailto:gary.mcintu...@esterline.com]
Sent: Thursday, June 13, 2013 3:24 PM
To: EMC-PSTC@LISTSERV.IEEE.ORG
Subject: [PSES] Pointer please.

Where in the safety directives are the instructions for spare parts or service 
parts. We manufacture a device for an end customer but don't do the safety 
approvals - we are just designated as a factory. I haven't seen any activity in 
getting this device approved under the new edition of the standard and am 
concerned that it has fallen through the cracks by the customer.
I don't believe it's a current production system but they are maintaining the 
systems already in the field, meaning that this are service parts I believe, 
but I don't know exactly what allows them to continue importing them into 
Europe.

The real issue is that some of the plastic that had been used in the past isn't 
going to be available but it is described as a critical component in the safety 
files by manufacturers name. model type. We can replace the material with the 
same flame rating but the raw material is from a different supplier. Even if 
spare parts are allowed for a system with an out of date harmonized safety 
standard I don't think one can just change the components without some 
activity, but exactly what and how, add some notes to the technical file?

I've tried discussing the issue with the customer but can't get through the 
purchasers to the compliance people, to insure that this isn't just slipping 
through the cracks.




Esterline Interface Technologies

Featuring
ADVANCED INPUT, GAMESMAN, LRE MEDICAL, and MEMTRON  products

600 W. Wilbur Avenue
Coeur d'Alene, ID  83815-9496
Toll Free: 800-444-5923 X1XXX
Tel:  (208) 635-8
Fax: (208) 635-8

www.esterline.com/interfacetechnologieshttp://www.esterline.com/interfacetechnologies

Technology, Innovation, Performance...
Information in or attached to this e-mail message may be subject to export 
control restrictions of the International Traffic in Arms Regulations (ITAR) 
(22 CFR pts. 120-130) or the Export Administration Regulations (EAR) (15 CFR 
pts. 730-774).  Before exporting this information outside the United States or 
releasing it to a foreign person in the United States, you need to determine 
whether a license under the EAR or the ITAR is required to do so.  If you have 
any questions about this obligation, please contact me.

Click 
herehttp://www.esterline.com/governance/email_disclaimer/tabid/1532/Default.aspx
 to read disclaimer




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Re: [PSES] Pointer please.

2013-06-13 Thread John Woodgate
In message 
d250d01e39356a4e9cc3b4b459d665509526c...@ms-cda-01.advanced-input.com, 
dated Thu, 13 Jun 2013, McInturff, Gary gary.mcintu...@esterline.com 
writes:


I've tried discussing the issue with the customer but can't get through 
the purchasers to the compliance people, to insure that this isn't just 
slipping through the cracks.


This is a political, not a technical  problem.

Tell them that you will (following professional advice) print in BIG RED 
LETTERS on invoices, delivery notes and instruction books (if you 
provide them) that the compliance is compromised by the substitution of 
an approved material.

--
OOO - Own Opinions Only. See www.jmwa.demon.co.uk
Why is the stapler always empty just when you want it?

John Woodgate, J M Woodgate and Associates, Rayleigh, Essex UK

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Re: [PSES] Pointer please.

2013-06-13 Thread John Woodgate
In message 
617eb8c8634c9149aa66c853d7b8ac5312e61...@by2prd0310mb389.namprd03.prod.o
utlook.com, dated Thu, 13 Jun 2013, Crane, Lauren 
lauren.cr...@kla-tencor.com writes:


It's a real mixed bag. I've heard the old Blue Guide is under revision. 
Maybe they will help clarify your question in it.


For me, the point is that if there were an incident, and the substitute 
material were discovered, Gary's company would be held liable if they 
had not disclosed the substitution. It is indeed of doubtful value to 
read the small print of the standards and Directives in such a case.


In fact, a case of 'conspiracy [with the customer] to conceal' might 
lie.

--
OOO - Own Opinions Only. See www.jmwa.demon.co.uk
Why is the stapler always empty just when you want it?

John Woodgate, J M Woodgate and Associates, Rayleigh, Essex UK

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