RE: OEM Issues (EU context)

2000-12-19 Thread Peter Merguerian

Dear All,

Who is liable? By purchasing a component that is CE marked will not satisfy
your needs! You need to check the technical file of the component to ensure
that it indeed meets the requirements. At the end of the day, you the
end-product manufacturer are liable for the overall CE and your people are
the ones spending time in jail!

Merry Xmas and Have a Happy and Safe New Year!


---Original Message-
From: owner-emc-p...@ieee.org [mailto:owner-emc-p...@ieee.org]On Behalf Of
wmf...@aol.com
Sent: Wednesday, December 13, 2000 5:03 PM
To: emc-p...@ieee.org
Subject: OEM Issues (EU context)



Similar to the 'SAFETY LISTING' thread this week:

As a manufacturer of electrical equipment, we purchase another manuf's power

supply, CE-marked by them with a copy of their Declaration of Conformance.
We 
then re-label it with our own label, make only minor physical changes, 
document the product and sell it in the EU. In the event that the unit's 
conformance to the Electromagnetic Compatibility Directive (89/336/EEC) or
to 
the Low Voltage Directive (73/23/EEC) is challenged, who is liable to 
represent the product? My guess is that we are ast least as responsible as 
the 'manufacturer', above, but mine is not a legal opinion.

Anyone out there (especially on the continent)in a position to offer advice 
on how I should proceed? 

Many thanks.

WmFlanigan

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RE: OEM Issues (EU context)

2000-12-13 Thread Grant, Tania (Tania)

Oh boy!   I do think you have a potential can of worms here.   I'll try and
take this one by one, my responses preceded by TG:


*   ...then re-label it with our own label, make only minor physical
changes, document the product and sell it in the EU.   TG:  I don't think
that you can legally re-brand someone else's product without their
permission.   Are you also attaching their existing regulatory approval
labels that are now associated with your name?   That is
misrepresentation, or worse.   Regarding ...minor physical changes..., you
may be sabotaging the power supply's existing safety approvals.  
*   In the event that the unit's conformance to the Electromagnetic
Compatibility Directive (89/336/EEC) or to the Low Voltage Directive
(73/23/EEC) is challenged, who is liable to
represent the product?  TG:   You are, since you are placing it on the
market.


Tania Grant,  tgr...@lucent.com
Lucent Technologies, Switching Solutions Group
Intelligent Network and Messaging Solutions


-Original Message-
From: wmf...@aol.com [ mailto:wmf...@aol.com mailto:wmf...@aol.com ]
Sent: Wednesday, December 13, 2000 7:03 AM
To: emc-p...@ieee.org
Subject: OEM Issues (EU context)



Similar to the 'SAFETY LISTING' thread this week:

As a manufacturer of electrical equipment, we purchase another manuf's power
supply, CE-marked by them with a copy of their Declaration of Conformance.
We
then re-label it with our own label, make only minor physical changes,
document the product and sell it in the EU. In the event that the unit's
conformance to the Electromagnetic Compatibility Directive (89/336/EEC) or
to
the Low Voltage Directive (73/23/EEC) is challenged, who is liable to
represent the product? My guess is that we are ast least as responsible as
the 'manufacturer', above, but mine is not a legal opinion.

Anyone out there (especially on the continent)in a position to offer advice
on how I should proceed?

Many thanks.

WmFlanigan

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RE: OEM Issues (EU context)

2000-12-13 Thread Brian O'Connell




As a manufacturer of electrical equipment, we purchase another manuf's
power 

supply, CE-marked by them with a copy of their Declaration of Conformance.
We 

then re-label it with our own label, make only minor physical changes, 

document the product and sell it in the EU. In the event that the unit's 

conformance to the Electromagnetic Compatibility Directive (89/336/EEC) or
to 

the Low Voltage Directive (73/23/EEC) is challenged, who is liable to 

represent the product? My guess is that we are ast least as responsible as 

the 'manufacturer', above, but mine is not a legal opinion.


If this p.s. is in any way accesable to the end user, and there are
conditions of usage on a CDF or an agency product test report, removal of
labels could have legal ramifications.


Std Disclaimer: anything I say or do may or may not have anything to do with
my employer's policies.

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RE: OEM Issues (EU context)

2000-12-13 Thread Ned Devine

Hi,

This is defined in some of the newer directives. i.e. the IVD Directive,
98/79/EC, Article 1, paragraph f.  I have to assume that what is a
manufacture in one directive is the same in all of the other directives.
They wouldn't have different definitions, for the same word, in different
directives would they? :-)

(f) 'manufacturer' means the natural or legal person with responsibility for
the design, manufacture, packaging and labelling of a device before it is
placed on the market under his own name, regardless of whether these
operations are carried out by that person himself or on his behalf by a
third party.  The obligations of this Directive to be met by manufacturers
also apply to the natural or legal person who assembles, packages,
processes, fully refurbishes and/or labels one or more ready-made products
and/or assigns to them their intended purpose as devices with a view to
their being placed on the market under his own name. This subparagraph does
not apply to the person who, while not a manufacturer within the meaning of
the first subparagraph, assembles or adapts devices already on the market to
their intended purpose for an individual patient;

Ned Devine
Entela, Inc.
Program Manager III
Phone 616 248 9671
Fax  616 574 9752
e-mail  ndev...@entela.com 



-Original Message-
From: acar...@uk.xyratex.com [mailto:acar...@uk.xyratex.com]
Sent: Wednesday, December 13, 2000 12:41 PM
To: wmf...@aol.com
Cc: emc-p...@ieee.org
Subject: Re: OEM Issues (EU context)



WmFlanigan

Our interpretation and how we always treat such issues is, as the seller of
the
equipment you are responsible to ensure it meets the requirements of the Low
Voltage and EMC directive. As you are re badging it, you will need to draw
up
your own DOCs. Off course you can base your conformity to the directives on
the
DOC provided with the original product. If you were not re badging, then no
new
DOC required.

Simple rule, if your name is on the front, you are claming responsibility
for the
product.

wmf...@aol.com wrote:

 Similar to the 'SAFETY LISTING' thread this week:

 As a manufacturer of electrical equipment, we purchase another manuf's
power
 supply, CE-marked by them with a copy of their Declaration of Conformance.
We
 then re-label it with our own label, make only minor physical changes,
 document the product and sell it in the EU. In the event that the unit's
 conformance to the Electromagnetic Compatibility Directive (89/336/EEC) or
to
 the Low Voltage Directive (73/23/EEC) is challenged, who is liable to
 represent the product? My guess is that we are ast least as responsible as
 the 'manufacturer', above, but mine is not a legal opinion.

 Anyone out there (especially on the continent)in a position to offer
advice
 on how I should proceed?

 Many thanks.

 WmFlanigan

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--

Andrew Carson - Product Safety Engineer
Xyratex Engineering Laboratory
Tele 023 92496855 Fax 023 92496014



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Re: OEM Issues (EU context)

2000-12-13 Thread Andrew Carson

WmFlanigan

Our interpretation and how we always treat such issues is, as the seller of the
equipment you are responsible to ensure it meets the requirements of the Low
Voltage and EMC directive. As you are re badging it, you will need to draw up
your own DOCs. Off course you can base your conformity to the directives on the
DOC provided with the original product. If you were not re badging, then no new
DOC required.

Simple rule, if your name is on the front, you are claming responsibility for 
the
product.

wmf...@aol.com wrote:

 Similar to the 'SAFETY LISTING' thread this week:

 As a manufacturer of electrical equipment, we purchase another manuf's power
 supply, CE-marked by them with a copy of their Declaration of Conformance. We
 then re-label it with our own label, make only minor physical changes,
 document the product and sell it in the EU. In the event that the unit's
 conformance to the Electromagnetic Compatibility Directive (89/336/EEC) or to
 the Low Voltage Directive (73/23/EEC) is challenged, who is liable to
 represent the product? My guess is that we are ast least as responsible as
 the 'manufacturer', above, but mine is not a legal opinion.

 Anyone out there (especially on the continent)in a position to offer advice
 on how I should proceed?

 Many thanks.

 WmFlanigan

 ---
 This message is from the IEEE EMC Society Product Safety
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  Richard Nute:   ri...@ieee.org

--

Andrew Carson - Product Safety Engineer
Xyratex Engineering Laboratory
Tele 023 92496855 Fax 023 92496014



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RE: OEM Issues (EU context)

2000-12-13 Thread Griffith, Monty J

The person who places the device on the market is ultimately responsible for
compliance with all directives. So you would be responsible to assure your
modifications do not affect the original compliance attributes.  

Thanks!!!

Monty Griffith
Test Engineer
INTERGRAPH FEDERAL SYSTEMS
Tel: (256) 730-4265
Fax:  (256) 730-6816
e-mail:  mjgri...@ingr.com
http://www.intergraph.com/govt/



-Original Message-
From: wmf...@aol.com [mailto:wmf...@aol.com]
Sent: Wednesday, December 13, 2000 9:03 AM
To: emc-p...@ieee.org
Subject: OEM Issues (EU context)



Similar to the 'SAFETY LISTING' thread this week:

As a manufacturer of electrical equipment, we purchase another manuf's power

supply, CE-marked by them with a copy of their Declaration of Conformance.
We 
then re-label it with our own label, make only minor physical changes, 
document the product and sell it in the EU. In the event that the unit's 
conformance to the Electromagnetic Compatibility Directive (89/336/EEC) or
to 
the Low Voltage Directive (73/23/EEC) is challenged, who is liable to 
represent the product? My guess is that we are ast least as responsible as 
the 'manufacturer', above, but mine is not a legal opinion.

Anyone out there (especially on the continent)in a position to offer advice 
on how I should proceed? 

Many thanks.

WmFlanigan

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RE: OEM Issues (EU context)

2000-12-13 Thread CE-test - Ing. Gert Gremmen - ce-marking and more...
Hello mr. Flanigan,

The one that actually sells the product on the European Market will be held
responsible.
I am not sure if you are USA based, but in that case your REP will get the
headache,
as well as bear all legal (and financial) consequences.  Hope for him he has
a decent
contract with you, hope for you you don't.:))

If you don't have a REP, well then it's your EC customer who is liable !
You'd better
have one anyway, to prevent being sued one day by one of your customer's.

Your REP will hold the (by him) signed DoC.

Regards,

Gert Gremmen, (Ing)

ce-test, qualified testing

===
Web presence  http://www.cetest.nl
CE-shop http://www.cetest.nl/ce_shop.htm
/-/ Compliance testing is our core business /-/
===


-Original Message-
From: owner-emc-p...@ieee.org [mailto:owner-emc-p...@ieee.org]On Behalf
Of wmf...@aol.com
Sent: Wednesday, December 13, 2000 4:03 PM
To: emc-p...@ieee.org
Subject: OEM Issues (EU context)



Similar to the 'SAFETY LISTING' thread this week:

As a manufacturer of electrical equipment, we purchase another
manuf's power
supply, CE-marked by them with a copy of their Declaration of
Conformance. We
then re-label it with our own label, make only minor physical changes,
document the product and sell it in the EU. In the event that the unit's
conformance to the Electromagnetic Compatibility Directive
(89/336/EEC) or to
the Low Voltage Directive (73/23/EEC) is challenged, who is liable to
represent the product? My guess is that we are ast least as
responsible as
the 'manufacturer', above, but mine is not a legal opinion.

Anyone out there (especially on the continent)in a position to
offer advice
on how I should proceed?

Many thanks.

WmFlanigan

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attachment: Gert Gremmen.vcf

OEM Issues (EU context)

2000-12-13 Thread WmFlan

Similar to the 'SAFETY LISTING' thread this week:

As a manufacturer of electrical equipment, we purchase another manuf's power 
supply, CE-marked by them with a copy of their Declaration of Conformance. We 
then re-label it with our own label, make only minor physical changes, 
document the product and sell it in the EU. In the event that the unit's 
conformance to the Electromagnetic Compatibility Directive (89/336/EEC) or to 
the Low Voltage Directive (73/23/EEC) is challenged, who is liable to 
represent the product? My guess is that we are ast least as responsible as 
the 'manufacturer', above, but mine is not a legal opinion.

Anyone out there (especially on the continent)in a position to offer advice 
on how I should proceed? 

Many thanks.

WmFlanigan

---
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