pr EN 50419 WEEE Marking Standard

2004-09-22 Thread Joe P Martin

Greetings, 

Is anyone aware of the status of prEN 50419 Marking of Electrical and
Electronic Equipment in accordance with article 11(2) of Directive 2002/96/EC
(WEEE)? Does anyone know where I can obtain a copy of this document? 

Your assistance is appreciated. 

Regards 

Joe Martin 
Applied Biosystems 
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Refurbished Products to EU

2003-11-18 Thread Joe P Martin





Greetings,

We are considering refurbishing laboratory equipment products that were
located in the EU.  These products will be removed from the EU and
refurbished.  Once the products are refurbished, we will be selling them to
new customers in the EU. The refurbishments will not include any "new"
technology.  I have a couple of questions for the group in regards to this
process.

1.Will the applicable regulatory requirements of "today" be required,
or the requirements from the original date of sale?
2.Are there any additional requirements for refurbished products?
2.Are there any specific labeling requirements to state that the
product has been refurbished?
3.Are there any type of reporting requirements to let Member States
know that we are performing this refurbishment and  reselling the
products in the EU? Would this requirement be different for products
self-certified versus products that requiredNotified Body Approvals
i.e. Medical, IVD etc.

As always, your responses are appreciated.

Regards

Joe Martin
Applied Biosystems
marti...@appliedbiosystems.com





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Re: LVD voltage limits

2003-11-05 Thread Joe P Martin





John,

The following link has the LVD Update #4.  This update followed a June 2003
Working Party Meeting.


http://www.europa.eu.int/comm/enterprise/electr_equipment/lv/direct/review.htm

Best Regards

Joe Martin
Applied Biosystems
marti...@appliedbiosystems.com



  
   
  "Tyra, John"
   
To:  
emc-p...@ieee.org   
  Sent by:  cc:   
   
  owner-emc-pstc@majordoSubject:  LVD voltage
limits  
  mo.ieee.org 
   
  
   
  
   
  11/05/2003 01:34 PM 
   
  Please respond to   
   
  "Tyra, John"
   
  
   
  
   




Hello Everyone,


I have read on this list and have been told by TUV that the lower limits
for the voltages of products which fall under the Low Voltage Directive may
be eliminated so that low voltage products would now fall under that
directive.


On the Europa website I read an LVD Working Document, dated 7/13/01, that
there were two proposals:

1. Delete the lower limit and introduce risk assessment similar to the
Machinery Directive
2. Leave the limits as is but add an annex to include certain low voltage
products, lighting system, household appliances, TV/Radio etc


I found a Working Guide for the LVD dated 3/7/02 which  showed that there
are countries which favor one or the other proposal while the UK favored no
change..


Does anyone have any new information or can point me in the direction which
would give me a more recent an update of this proposal? I am very
interested in where this proposal is heading..


Thanks in advance for your help..


Regards,





John Tyra
Product Safety and Regulatory Compliance Manager


Bose Corporation
The Mountain, MS-450
Framingham, MA 01701-9168
Phone: 508-766-1502
Fax: 508-766-1145
john_t...@bose.com








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Regulatory Plan

2003-10-21 Thread Joe P Martin





Greetings,

I have been asked to put together a regulatory plan for one of our
company's products.  I am trying to get as many opinions as possible as to
the elements of such a plan. Please share with me your elements of such a
plan and, if possible, send me a copy of a plan to use as an example.

Your assistance is greatly appreciated.

Regards

Joe Martin
Applied Biosystems
marti...@appliedbiosystems.com



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New Approach vs WEEE/RoHS

2003-07-02 Thread Joe P Martin

Greetings,

It is my understanding that the WEEE and RoHS Directives are not New
Approach Directives.  What is the difference between New Approach
Directives and other directives such as WEEE/RoHS?

In order to declare conformity to New Approach Directives, the manufacturer
places the CE mark on the product and issues a Declaration of Conformity.
How does a manufacturer declare compliance to the WEEE/RoHS?

As always, your responses are appreciated.

Regards

Joe Martin
EMC/Product Safety Engineer
Applied Biosystems
marti...@appliedbiosystems.com






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IVDD Seminars

2003-07-01 Thread Joe P Martin

Greetings,

I am looking for an IVDD Seminar located in the California/San
Francisco/San Jose area.

All leads are appreciated.

Regards

Joe Martin
Applied Biosystems
marti...@appliedbiosystems.com




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Lab Equipment/WEEE RoHS

2003-06-11 Thread Joe P Martin

Greetings

I am trying to determine whether our laboratory equipment is required to
comply with the RoHS and WEEE Directives at this time.
We do have some instruments for use as IVD and realize that they do fall
under the scope of the WEEE Directive as Category 8 "Medical Devices:
Laboratory
Equipment for in-vitro diagnosis."  However, we are not sure about our
thermal cyclers, DNA sequencers, mass spectrometers, etc.

The scope currently includes Category 9 called "Monitoring and Control
Instruments" and gives examples including "Measuring, weighing, or
adjusting appliances for household or as laboratory equipment".   Our
instruments do not seem like any of the other examples for the same
category, yet they do measure things.  Our mass spectrometers can use
flight time of ions to help determine the mass and thus the original
constitution of the sample.

In addition, Member States may specify laboratory equipment within their
laws that support the WEEE Directive. As an example, the current Swedish
WEEE laws on producer responsibility clearly states that laboratory
equipment is included.

Your thoughts on this subject are appreciated.

Regards

Joe Martin
Applied Biosystems
marti...@appliedbiosystems.com




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ENV 50204

2003-05-21 Thread Joe P Martin

Greetings,

ENV 50204 is titled "Radiated Electromagnetic Fields from Digital Radio
Telephones-Immunity Test"

Please refresh my memory on what exactly is an "ENV" Standard?  Are there
any requirements for testing to ENV's?  For what type of products would ENV
50204  be applicable?

We normally test to EN 61326.  It has been some time since I looked at EN
50082-1 Generic Immunity.  Could someone be so kind as to list what
immunity standards are in the latest version of EN 50082-1.  Does the
latest version still state that if there is a product specific standard
then that standard takes precedence over the generic standard?

Your responses are greatly appreciated.

Regards

Joe Martin
Applied Biosystems
marti...@appliedbiosystems.com








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Re: D of C again

2003-04-30 Thread Joe P Martin


Greetings,

The statement below is not correct for all Directives.

The EMC Directive Guidelines states: " Where neither the manufacturer nor
his authorised representative is established within the EEA, the obligation
to keep the technical documentation available is the responsibility of the
person who places the apparatus on the EEA market."  The requirement is the
same for the D of C.

The EMC Directive Guidelines also states "It is not a requirement of this
Directive to supply a declaration of conformity with the apparatus."

Since these requirements vary by Directive, it is important to review the
specific Directives.

Regards

Joe Martin
Applied Biosystems



  
  
Douglas_Beckwith@MITEL.   
  
com   To: lfresea...@aol.com  
  
Sent by:  cc:
emc-p...@majordomo.ieee.org
owner-emc-pstc@majordom   Subject: Re: D of C
again  
o.ieee.org
  
  
  
  
  
04/29/2003 08:18 AM   
  
Please respond to 
  
Douglas_Beckwith  
  
  
  
  
  






And the answer is

The D of C must be signed by the responsible person designated by the
manufacturer. The signatory does not have to be located in the EU.
The manufacturer must designate a representative in the EU who will hold
the certificate and the technical file. This could be an agent,
distributor.
A copy of the D of C that states the directives complied with must be
placed in the user manual. Note, this does not have to be signed, but it
must state where the signed original can be obtained. i.e. the EU
representative's contact details.


Doug Beckwith

(OOPO)



lfresea...@aol.com

Sent by: To:
emc-p...@majordomo.ieee.org
owner-emc-pstc@majordom  cc:

o.ieee.org   Subject: D of C again



04/29/03 09:13 AM

Please respond to

Lfresearch







Hi folks,

I've been asked by a US manufacturer who's signature if any should appear
on the D of C, and should they be located on European soil.

Is there a clear consensus?

Thanks,

Derek N. Walton
Owner L F Research EMC Design and Test Facility
Poplar Grove,
Illinois,  USA
www.lfresearch.com





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Competent Authority Registration

2003-04-22 Thread Joe P Martin

Greetings,

The In-Vitro Diagnostics Directive requires that any manufacturer who
places a device on the market notify the competent authorities of the
Member State(s) in which he has his registered place of business.  I have a
couple of questions in regards to this requirement.

1.   Does this mean that we have to register with every regulatory
authority in all Member States, or is registration with one Member State
sufficient?  The product  is not manufactured in the EU, yet we do have
places of business in several Member States.

2.   For General IVD devices, how does a U.S. manufacturer register their
product in Europe?

3.   Does anyone have a list of the regulatory authorities for all Member
States?

As always, your responses are greatly appreciated.

Regards

Joe Martin
Applied Biosystems
marti...@appliedbiosystems.com





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Is Authorised Representative in EU Required?

2003-03-25 Thread Joe P Martin

Greetings,

In order to meet the requirements of European Union Directives, if the
manufacturer is not established in the Community, is it required to have an
Authorised Representative established in the Community?  Is the
requirement, or non-requirement, the same for all Directives?  I am mostly
concerned with In-Vitro Diagnostics, EMC, Low Voltage, Machinery and
Medical Directives. If you have available, please provide specific
Article(s) where this is specified in the Directives or the Directive
Guidelines.

As always, your responses are greatly appreciated.

Regards

Joe Martin
Applied Biosystems
marti...@appliedbiosystems.com



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Global Chemical Regulations Forum?

2003-02-25 Thread Joe P Martin

Greetings,

Is anyone aware of a forum, similar to the EMC-PSTC forum, that deals with
Global Chemical Regulations?

All responses are appreciated.

Regards

Joe Martin
Applied Biosystems
marti...@appliedbiosystems.com



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Custom Units in EU

2003-02-19 Thread Joe P Martin

Greetings,

We are planning to manufacture up to 50 units for laboratory use.  Each of
these units will be one of a kind.  These units will be shipped to the EU
to our own laboratory and operated by our personnel.  If I recall correctly
there are exemptions for one of a kind units for EMC, LVD and Machinery
Directives.  However, I was unable to locate this information in the
guidelines to these Directives.  Can members of the group provide me with
specific information regarding the requirements, if any, for one of a kind
units located in the manufacturers facility and operated by employees of
the manufacturer in the EU?

All responses are appreciated.

Regards

Joe Martin
Applied Biosystems
marti...@appliedbiosystems.com



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Member States versus EU

2003-02-05 Thread Joe P Martin

Greetings,

If Member States of the European Union have existing laws in place that
conflict with, or are in addition to, European Union Directives, do the
Member States have to amend their laws to be in line with the Directives?

Any and all responses are appreciated.

Regards

Joe Martin
Applied Biosystems



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Sweden WEEE Requirements

2003-02-04 Thread Joe P Martin

Group,

Sweden's Ordinance on Producer Responsibility for waste from electronic
equipment has been in effect since July 1, 2001.  The requirements are not
the same as the upcoming European Union WEEE Directive. I have several
questions for the group.

Why do you think the Swedish requirements have never been discussed on this
forum?
How is your company addressing the Swedish requirements?
Will the Swedish requirements need to be updated to meet the WEEE Directive
requirements?
The Swedish requirements specifically list "Laboratory Equipment" as having
to comply with their requirements.  The WEEE Directive does not list
laboratory equipment in it's scope.  Will this discrepancy need to be
clarified?
Can individual member states have different requirements than the EU
requirements?
Do other member states have individual WEEE requirements at this time?

All responses are appreciated.

Regards

Joe Martin
Applied Biosystems
marti...@appliedbiosystems.com






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NRTL in the U.S.

2003-01-14 Thread Joe P Martin

Greetings,

As has been discussed in previous threads, NRTL Listing is not a
requirement to sell electronic products in the U.S.  However, there are
cities, counties, etc. within the U.S. that do require NRTL Listing.
These include Los Angeles and Chicago.  Does anyone have a comprehensive
list of all the cities, counties or states that do require NRTL Listing.

Any and all comments are appreciated.

Regards

Joe Martin
Applied Biosystems
marti...@appliedbiosystems.com




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Canadian EMC Labeling Exemptions

2002-12-17 Thread Joe P Martin

Greetings,

Are there any exemptions that allow Canadian manufacturers to disregard the
product labeling or statement in the user's manual for indicating
compliance with ICES-001 or ICES-003.

All responses are appreciated.

Regards

Joe Martin
marti...@appliedbiosystems.com


---
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RoHS/WEEE and Laboratory Equipment

2002-10-30 Thread Joe P Martin

Greetings,

The scope of the RoHs and WEEE Directives states that the Directives apply
to equipment specified in Annex 1A of the WEEE Directive.  Annex 1B of the
Directive gives specific products under the categories in Annex 1A.
Category 8 is Medical Devices.  Included in this category is "Laboratory
equipment for in-vitro diagnostics".  However, the category does not
include "Laboratory Equipment".  The Directive also states that "This
Directive should cover all electrical equipment used by consumers and
electrical and electronic equipment intended for professional use which
might end up in the municipal waste system".

In your opinion, have they exclude "Laboratory Equipment" from these
requirements?  If so, why?

Your responses are appreciated.

Regards

Joe Martin
EMC/Product Safety Engineer
marti...@appliedbiosystems.com




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WEEE/RoHS Directives

2002-10-16 Thread Joe P Martin

Greetings,

Have the WEEE and RoHs Directives been officially accepted by the EU?  Does
anyone know where I can obtain the latest copies of these Directives? The
latest I found on the Europa site was a proposal draft dated June 2000.  I
also found copies on the Industry Council for Electronic Equipment
Recycling site dated 2001(Not sure what month).  I also read that there was
an amendment dated in 2002 that changed the implementation date of the RoHS
Directive from 2007 to 2006.

Any recent information on these Directives is greatly appreciated.

Regards

Joe Martin
Applied Biosystems
marti...@appliedbiosystems.com


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Re: EN61000-3-2

2002-09-24 Thread Joe P Martin


Cecil,

To make it less confusing, use the 2nd edition.  EN 61000-3-2 Ed. 2:2000.

The 2nd edition supersedes EN 61000-3-2: 1995 + A1: 1998 + A2: 1998 +
A14:2000.

Regards

Joe Martin
Applied Biosystems





  
cecil.gitt...@kodak.com 
  
Sent by:   To: 
emc-p...@majordomo.ieee.org
owner-emc-pstc@majordomcc:  
  
o.ieee.org Subject: EN61000-3-2 
  

  

  
09/24/2002 12:41 PM 
  
Please respond to   
  
cecil.gittens   
  

  

  





Does anyone have knowledge on how the standard EN61000-3-2 should be
listed?
Is it EN61000-3-2:1995, EN61000-3-2:1995 A2:1998 or EN61000-2-3:1995
A14:2000?

Regards

Cecil A. Gittens





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Compliance Engineering Position

2002-09-19 Thread Joe P Martin

Greetings,



The Applied Biosystems Division located in the Houston Texas area has the
following opening in the Compliance Engineering Department:

Duties include leading EMC and product safety engineering functions,
including working with manufacturing and R&D to determine requirements for
implementing and monitoring regulations.  Collect and analyze data that
help determine compliance engineering issues, trends and improvements.

This position requires the knowledge and skills normally acquired through
the successful completion of a BSEE degree and/or
electronics background.  3-7 years product safety and/or EMC experience
preferred.  Computer literate.  Understanding of manufacturing
processes.  Minimum 5 years experience demonstrating communication,
organization and engineering skills.

Please forward your resumes directly to:

Joe Martin
Applied Biosystems
marti...@appliedbiosystems.com
850 Lincoln Centre Dr.
Foster City, CA 94404
(650) 638-5695




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Re: Immunity severity levels

2002-09-19 Thread Joe P Martin



Alan,

Level 1:  (1V/M)Low-level electromagnetic radiation environment.
Levels typical of local radio/television stations located at more than 1
km, and transmitters/receivers of low power.

Level 2:  (3V/M)Moderate electromagnetic radiation environment.  Low
power portable transceivers (typically less than 1 W rating) are in use,
but with restrictions on use in close proximity to the equipment.  A
typical commercial environment.

Level 3:  (10V/M)   Severe electromagnetic radiation environment.  Portable
transceivers (2 W rating or more) are in use relatively close to the
equipment but not less than 1m.   High power broadcast transmitters are in
close proximity to the equipment and ISM equipment may be located close by.
A typical industrial environment.

Level x:  (Special) Level x is an open level which might be negotiated and
specified in the product standard or equipment specification.

Regards

Joe Martin
Applied Biosystems




  
alan.hud...@amsjv.com   
  
Sent by:   To: 
emc-p...@majordomo.ieee.org
owner-emc-pstc@majordomcc:  
  
o.ieee.org Subject: Immunity 
severity levels  

  

  
09/18/2002 10:14 AM 
  
Please respond to   
  
alan.hudson 
  

  

  






With regard to radiated emission immunity and EN61000-4-3 (or IEC 801-3)
I believe there are different field strengths used, depending on the
environment in which the apparatus being tested is to be used.

I believe equipment to be used in a well-protected environment may be
tested at a lower immunity level than equipment to be used in an
unprotected environment.

I've ordered a copy of 61000-4-3, but while I'm waiting I'd like to know
ASAP:

1) What are the definitions of the levels?
2) What field strengths  are used for the various levels? (I think level
2 is 3V/m and level 3 is 10V/m)

Regards,

Alan


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Re: Immunity severity levels

2002-09-18 Thread Joe P Martin


Alan,

Level 1:  (1V/M)Low-level electromagnetic radiation environment.
Levels typical of local radio/television stations located at more than 1
km, and transmitters/receivers of low power.

Level 2:  (3V/M)Moderate electromagnetic radiation environment.  Low
power portable transceivers (typically less than 1 W rating) are in use,
but with restrictions on use in close proximity to the equipment.  A
typical commercial environment.

Level 3:  (10V/M)   Severe electromagnetic radiation environment.  Portable
transceivers (2 W rating or more) are in use relatively close to the
equipment but not less than 1m.   High power broadcast transmitters are in
close proximity to the equipment and ISM equipment may be located close by.
A typical industrial environment.

Level x:  (Special) Level x is an open level which might be negotiated and
specified in the product standard or equipment specification.

Regards

Joe Martin
Applied Biosystems




  
alan.hud...@amsjv.com   
  
Sent by:   To: 
emc-p...@majordomo.ieee.org
owner-emc-pstc@majordomcc:  
  
o.ieee.org Subject: Immunity 
severity levels  

  

  
09/18/2002 10:14 AM 
  
Please respond to   
  
alan.hudson 
  

  

  






With regard to radiated emission immunity and EN61000-4-3 (or IEC 801-3)
I believe there are different field strengths used, depending on the
environment in which the apparatus being tested is to be used.

I believe equipment to be used in a well-protected environment may be
tested at a lower immunity level than equipment to be used in an
unprotected environment.

I've ordered a copy of 61000-4-3, but while I'm waiting I'd like to know
ASAP:

1) What are the definitions of the levels?
2) What field strengths  are used for the various levels? (I think level
2 is 3V/m and level 3 is 10V/m)

Regards,

Alan


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Re: Clock frequencies

2002-09-18 Thread Joe P Martin



Neil,

Section 15.33  of FCC Part 15 "Frequency Range of Radiated Measurements"
provides you with this information.

Regards

Joe Martin
Applied Biosystems




  
Neil Helsby 
  
cc:  
  
Sent by:   Subject: Clock 
frequencies 
owner-emc-pstc@majordom 
  
o.ieee.org  
  

  

  
09/18/2002 03:53 AM 
  
Please respond to Neil  
  
Helsby  
  

  

  





I read somewhere, and now cannot find, a reference to FCC requirements
with respect to the relationship between clock frequency and highest
emissions scan frequency.

Can anyone help, preferably pointing to the FCC document?

I also seem to remember similar comments being considered by the EU. Can
anyone advise on these?

Many thanks,

Neil Helsby


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Re: Clock frequencies

2002-09-18 Thread Joe P Martin


Neil,

Section 15.33  of FCC Part 15 "Frequency Range of Radiated Measurements"
provides you with this information.

Regards

Joe Martin
Applied Biosystems




  
Neil Helsby 
  
cc:  
  
Sent by:   Subject: Clock 
frequencies 
owner-emc-pstc@majordom 
  
o.ieee.org  
  

  

  
09/18/2002 03:53 AM 
  
Please respond to Neil  
  
Helsby  
  

  

  





I read somewhere, and now cannot find, a reference to FCC requirements
with respect to the relationship between clock frequency and highest
emissions scan frequency.

Can anyone help, preferably pointing to the FCC document?

I also seem to remember similar comments being considered by the EU. Can
anyone advise on these?

Many thanks,

Neil Helsby


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Water + Electricity

2002-09-11 Thread Joe P Martin

Greetings,

A friend of mine is teaching elementary school students on the dangers of
mixing water with electricity.  However, he also wants to show examples of
situations where water and electricity mix, yet does not cause a problem.
Does anyone have any examples?

Also, does anyone have a great elementary school explanation as to what
elements or conditions are needed to be present before water and
electricity become dangerous?

All responses are appreciated.

Joe Martin
Applied Biosystems
marti...@appliedbiosystems.com


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Re: question on capacitor discharging

2002-08-28 Thread Joe P Martin


Susan,

For Laboratory Equipment, section 6.10.3 (c) of UL 3101-1, EN 61010-1 and
CSA 1010.1 states  "If plug pins of cord connected equipment receive a
charge from an internal capacitor, the pins shall not be hazardous live 5s
after disconnection of the supply".

Regards

Joe Martin
Compliance Engineering
Applied Biosystems




  
 To: emc-p...@ieee.org
  
Sent by:   cc:  
  
owner-emc-pstc@majordomSubject: question on 
capacitor discharging 
o.ieee.org  
  

  

  
08/28/2002 07:51 AM 
  
Please respond to   
  
shbeard 
  

  

  





Hello to all,
Other than MIL-HDBK-454 which states (as a guide) that "high voltage
circuits and capacitors should be provided with discharging devices unless
they discharge to 30 volts or less within 2 seconds after power removal"
are there other standards that specify/require capacitors to be discharged
to a certain voltage within a specified time?

Thanks,
Susan Beard
EMI Engineer



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Re: EMC Directive

2002-08-21 Thread Joe P Martin


John,

Article 7 in the Directive discusses using national standards to meet the
protection requirements of the Directive.  The Directive does not go into
detail on DOW's of the standards.  Take a look at the "Guide to the
implementation of directives based on the New Approach and the Global
Approach"  Section 4.5 discusses revisions to the standards. It states
"...the relevant European standard organisation lays down the date of
publication at national level of the revised harmonised standard, and the
date of withdrawal of the old standard.   The transitional period is
normally the time period between these two dates.  During this transitional
period, both harmonised standards give presumption of conformity, provided
that the conditions for this are met.  After this transitional period, only
the revised harmonised standard gives a presumption of conformity."

These guidelines can be downloaded from the following site.

http://europa.eu.int/comm/enterprise/newapproach/legislation/guide/document/1999_1282_en.pdf



Regards

Joe Martin




  
John Juhasz 
  
  
gix.com>   cc:  
  
Sent by:   Subject: EMC Directive   
  
owner-emc-pstc@majordom 
  
o.ieee.org  
  

  

  
08/21/2002 10:09 AM 
  
Please respond to John  
  
Juhasz  
  

  

  





I know this has come up before, but I need to quote chapter and verse.

In a conversation with an acquaintance of mine, the EMC Directive became a
topic with
DoW and use of superceded standards for presumption of conformity becoming
a
contentious area.
I maintain the following understanding:

A product is evaluated to standard A. At some point standard a can no
longer
be used for
presumption of conformity (DoW) and standard B must be used. Therefore if a
product is
still being manufactured for sale after the DoW of standard A, then the
product must
be re-evaluated according to the new standard B. (An exemption being those
items
returned for repair and not modified/updated/upgraded).
If the product was no longer produced and placed on the market after the
DoW
then
there is no issue.

My acquaintance notes that if the product was tested to standard A, as long
as it
has not been 'updated, modified, or changed in anyway' since the initial
compliance
test, it can still be manufactured and placed on the market after the DoW
without
re-test.

I believe that my understanding is the correct one. I tried to locate it in
the EMC
Directive itself but I can't seem to find it. Am I incorrect?

John A. Juhasz

GE Interlogix
Fiber Options Div.
Bohemia, NY






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Re: Emissions "quick test"

2002-08-21 Thread Joe P Martin


Lisa,

If you are just interested in "sniffing" out emissions, Credence
Technologies manufactures a probe with a built in low noise amplifier.  You
can use this probe without a spectrum analyzer to "sniff" out emissions.
However, unless you connect the probe to a spectrum analyzer, you can not
determine emission levels.  If you are interested, take a look at their
website.

http://www.credencetech.com/scanem.html

Regards

Joe Martin




  
lisa_cef...@mksinst.com 
  
Sent by:   To: 
emc-p...@majordomo.ieee.org
owner-emc-pstc@majordomcc:  
  
o.ieee.org Subject: Emissions 
"quick test"

  

  
08/20/2002 01:34 PM 
  
Please respond to   
  
Lisa_Cefalo 
  

  

  





Hi all,

Does anyone know of a " down- and- dirty" , inexpensive method or equipment
for sniffing out emissions issues?  I've used a Spectrum Analyzer in the
past with a series of different probes, but that tends to be costly.  Also,
Is there a "universal" probe kit out there?

Thank you in advance.

Lisa

Lisa A. Cefalo, CRE
Manager, Reliability and Design Services
MKS Instruments
6 Shattuck Road
Andover, MA 01810
(978)-975-2350  X 5669
lisa_cef...@mksinst.com


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Canadian EMC

2002-08-14 Thread Joe P Martin

Greetings,

Canadian EMC standard for ISM equipment is defined in ICES-001 Issue 3
1998.  Similarly, the EMC standard for digital apparatus is defined in
ICES-003 Issue 3 1997.  These standards are based on CISPR requirements.

Are these standards required by Industry Canada or are they voluntary.  If
they are required, where is this information specified?

All responses are appreciated.

Regards

Joe Martin
Applied Biosystems
marti...@appliedbiosystems.com






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Re: Online Standards EN61010-1

2002-08-07 Thread Joe P Martin


Doug,

The IEC document is identical to the EN version as stated in EN
61010-1:2001  "The text of the International Standard IEC 61010-1:2001 was
approved by CENELEC as a European Standard without any modifications."

Regards

Joe Martin
Applied Biosystems





  
"POWELL, DOUG"  
  
  To: "EMC-PSTC (E-mail)" 

Sent by:   cc:  
  
owner-emc-pstc@majordomSubject: Online 
Standards EN61010-1
o.ieee.org  
  

  

  
08/07/2002 10:15 AM 
  
Please respond to   
  
"POWELL, DOUG"  
  

  

  





Hello all,

I have been searching for a document service that has electronic format
standards (PDF) for EN61010-1:2001 with fully functional text search.  IHS
Global and TechStreet have hardcopy only.  BSI offers electronic but it's
only a converted TIFF format.  I thought about using the IEC but I am not
sure if there are any national deviations in the European Norm.

Any help you can provide is appreciated.


-doug

---
Douglas E. Powell, Compliance Engineer
Advanced Energy Industries, Inc.
Ft. Collins, CO 80525
mailto:doug.pow...@aei.com
---




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European FDA Equivalent

2002-08-07 Thread Joe P Martin

Is there a European and/or Canadian equivalent to the FDA in the US in
regards to diagnostic medical equipment?  If so, what are the organizations
names and are their requirements similar to the FDA's?

Any assistance is appreciated.

Regards

Joe Martin
Applied Biosystems
marti...@appliedbiosystems.com



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EN 60825 Laser Classifications

2002-08-07 Thread Joe P Martin

Group,

Amendment 2 (2001) to EN60825 Safety of laser products, has changed some
laser classifications.  The amendment has included new classifications 1M,
2M and 3R.  Class 1M and 2M include in their definitions " For diverging
beams if the user places optical components within 100mm from the source to
concentrate the beam..."  What is the rational of adding these
classifications?  What is an example of a product that would use this
technology?  Why did the IEC choose the letters "M" and "R" for these new
classifications?

All responses are greatly appreciated.

Regards

Joe Martin
Applied Biosystems


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In-Vitro Diagnostic Equipment

2002-08-01 Thread Joe P Martin

Greetings,

We currently manufacture and market a product as laboratory equipment not
intended for diagnostic purposes.  This product has been evaluated to EN
61010-1, EN 61326, CSA  1010.1 and UL 3101-1.

We are considering marketing this product as an "In-vitro diagnostic"
device.  Do we need to re-evaluate this product to a different set of
standards?  If so, which Directives/standards are applicable.

All responses are greatly appreciated.

Regards

Joe Martin
Applied Biosystems
marti...@appliedbiosystems.com


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Re: "made in xxxx" requirements?

2002-07-23 Thread Joe P Martin


Brent,

I did some research on this subject a while back.  The following web sites
should be helpful:

US International Trade Commission  http://www.usitc.gov/sec/I0619S3.HTM

The Trade Information Center   http://www.ita.doc.gov/td/tic/

US Department of Commerce  http://home.doc.gov

Federal Trade Commission
http://www.ftc.gov/os/1997/9712/epsmadeusa.htm
http://www.ftc.gov/opp/jointvent/madeusa/factsht.htm

US Customs Trade Office  (202) 927-0300

If you would like more info, give me a call or email

Regards

Joe Martin
Applied Biosystems
(650) 638-5695
marti...@appliedbiosystems.com





  
brent.dewitt@us.datex-o 
  
hmeda.com  To: 
emc-p...@majordomo.ieee.org
Sent by:   cc:  
  
owner-emc-pstc@majordomSubject: "made in " 
requirements?  
o.ieee.org  
  

  

  
07/18/2002 04:22 PM 
  
Please respond to   
  
brent.dewitt
  

  

  





This is not my usual area of interest, but a question came up about
regulations for country of origin marking, either in the US or EU.  Can
anyone point me in the direction of an answer?

Thanks all,

Brent DeWitt
Datex-Ohmeda
Louisville, CO


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EMC Directive/Repaired Apparatus

2002-07-17 Thread Joe P Martin

To all,

The following scenario is in regards to the EMC Directive.

We are a manufacturer located in the US.  We have various products that
were placed on the EU market prior to the enforcement of the EMC Directive.
We need to repair some of these products.  The repairs will not modify the
product to an "as new" piece of apparatus.  We want to have the products
repaired in the US.

Questions:

1.   Following the repairs, do we need to meet the requirements of the
Directive?  If so, why?
2.   If not, how do we get the products back into the EU without the CE
Marking?

Hopefully someone has had some experience with this issue.

All responses are appreciated.

Regards

Joe Martin
EMC/Product Safety Engineer
Applied Biosystems
marti...@appliedbiosystems.com


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