RE: Define Continuous DC Voltage - defibrillation

2001-11-20 Thread robertj
For those who want to skip it, this is not product safety, just a
digression from the electric shock topic.
 
As for why the chest thumping works, take the heel of your hand and
whack yourself on the side of the head. You'll notice the effect as
quite a few cells depolarize. That's the general idea. If you get the
heart's attention without doing serious damage, it may pause and
restart.
 
As for the PQRST stuff, you asked for it. Now we are getting into vector
graphics. Picture two cells, side by side, and depolarize one. You can
imagine a time related voltage vector appear and go away. Now picture
more cells, and depolarization flowing in a wave across them. The vector
gets more interesting both in direction and time. Next, go to three
dimensions and place it in a chest. That's what we are working with. Put
electrodes on the arms and watch it on a scope and you will get an EKG.
Of course you only have one dimension (plus time) represented on the
scope. Lets try a few more to get images of that vector in other
dimensions. In fact, we do it twelve times to get the standard 12 lead
EKG recording. Namely:
I - left arm to right arm
II - left foot to right arm
III - left foot to left arm
AVR - right arm to (feet, left arm)
AVL - left arm to (feet, right arm)
AVF - left foot to (arms, right foot)
V1 thru V6 - measurements from leads spread across the chest from
between the nipples to the right of the sternum around beneath the left
breast to the side of the chest. Each lead one at a time is measured to
all limb leads connected together.
 
If you can picture it, the first six measurements give six vector
readings in the plane of the limbs, the second six give vector readings
in a quadrant cross section of the chest perpendicular to the first six.
You actually get a pretty good set of three dimensional readings.
 
Now. Put an arrow through a board, throw it in the ocean and watch what
it does as a nice wave goes by. Describe the motion of that vector to
someone and see if he can deduce what the wave looks like. Its not
random. As each similar wave goes by, you get the same vector path. You
can even match vector paths with different types of waves.
 
That's what we do with an EKG. In fact there is a connection between
heart activity and the waveshape. However it's sort of remote. What
really happens is, we find a normal heart generates a typical pattern.
Consider heart disease like an AV block and the pattern changes. That's
what its all about. Pattern recognition. A good electrocardiologist has
this immense image recognition system in his head and matches EKG
patterns to disease. He will in fact generate a picture of where the
vector is pointing in time and space and use it to imagine weak or
damaged tissue affecting or modifying its path.
 
All that leads to the scope trace and talking about it. If we take the I
lead as the typical view and start describing it time wise, we start
with 
P, a small positive hump which corresponds with the atrial contraction
Q R  S, the negative, positive, negative pulse caused by ventricular
contraction and the movement of the voltage vector during that time.
T, another smaller slower hump from the repolarization of the ventricles
 
I can't help mentioning an EKG machine I once had which was absolutely
amazing. It had NO amplifiers. It was called an Einthoven string
galvanometer. It consisted of a large C shaped magnet whose poles
tapered down to a very narrow gap. Between that gap stretched a fine
gold plated glass fiber which connected to the attenuator (that's right
attenuator) and lead selector. There was a hole drilled from the top of
the C through the tips of the poles and out the bottom with a light
source on one side and moving photo film on the other. It produced a
strip chart recording of the movement of the fiber, which of course was
the EKG current deflected by the magnetic field. The machine used
electricity, for the light bulb and the film motor. It's amazing to
think of the skill and ingenuity used to make a millivolt recorder back
in those days. If I'm not mistaken, Einthoven was the inventor of the 12
lead EKG recording technique.
 
Bob Johnson
 
-Original Message-
From: Bill Owsley [mailto:ows...@cisco.com] 
Sent: Tuesday, November 20, 2001 12:53 PM
To: robertj; 'Bill Owsley'; 'Gary McInturff'; 'Gregg Kervill'; 'Rich
Nute'
Cc: jrbar...@lexmark.com; emc-p...@majordomo.ieee.org
Subject: RE: Define Continuous DC Voltage - defibrillation
 
excellent - now if you'll go through the PQRST complex also...

- Bill

Robert,
Thanks for this very interesting piece of data. I've often wonder
what atrioventricular fibrillation is, you provide some insight on that
as well.
If it is a reset of sorts then how did the thumping of the chest
ever work? I suppose it can also fall into the category of just being
better than nothing at all. 
I can be learned wrong and always look for a better understanding.
Its been awhile but I believe the information came from one 

RE: Methods Equipment; Surge Dips

2001-11-20 Thread Mike Hopkins
To answer the below -- KT has had the equipment for about 10 years.
For rental -- call Transient Specialists at 866-364-7368.
For robustness -- need to know the load. Large in-rush currents are
generally no problem.
I agree about the Pacific Power units -- we evaluated them here some years
ago -- they were one of the few AC sources that weren't upset with
transients on the output stage coming back from an EUT.
 
Mike Hopkins

-Original Message-
From: Ehler, Kyle [mailto:keh...@lsil.com]
Sent: Tuesday, November 20, 2001 3:57 PM
To: 'Mike Hopkins'; Ehler, Kyle; 'wmf...@aol.com'; emc-p...@ieee.org
Subject: RE: Methods  Equipment; Surge  Dips


True, but did KT have this equipment 4yrs ago?
Does anyone you know of rent this equipment?
 
We also have a Schaffner tap switcher, but it eats itself under heavy loads.
Is the KT stuff more robust under heavy startup loads?
The Pacific Power equipment I use has never broke down.  Worth the weight
just for that...
kyle

-Original Message-
From: Mike Hopkins [mailto:mhopk...@thermokeytek.com]
Sent: Tuesday, November 20, 2001 2:47 PM
To: 'Ehler, Kyle'; 'wmf...@aol.com'; emc-p...@ieee.org
Subject: RE: Methods  Equipment; Surge  Dips


Seems to me this is the hard way to do it. 
KeyTek has a product that is a tap switcher for the required levels and will
pass the in-rush currents required. It's a much smaller package.
 
Also, other manufacturers have systems that are basically software
controlled switches -- bring in the AC levels you require via a variac or
some other transformer and simply switch between them
 
Mike Hopkins

-Original Message-
From: Ehler, Kyle [mailto:keh...@lsil.com]
Sent: Tuesday, November 20, 2001 1:19 PM
To: 'wmf...@aol.com'; emc-p...@ieee.org
Subject: RE: Methods  Equipment; Surge  Dips



Hi William, 
I dont know about renting equipment for the tests. 
You can probably find it. 

For the -4-11 (dip/dropout) test; 
Depending on your load, your site wiring has to be up to snuff. 
The power sources for doing the dip and dropout test are hefty stuff. 
My lab uses a three-phase powered source to deliver a max of 16A into a
single phase capacitive (SMPS) load. 
I have a Pacific Power 140 TMX and an AMX 390.  The 140 does
flicker/harmonics and can do dip/dropout within its output limits (about 10A
inrush).  Any loads beyond a 10A inrush gets dip/dropout tested by the 390.
The 140 is totally pc controlled but can be programmed through the front
panel.  It is a handy doer.

The 390 is the heavy (up to 20A inrush) and I program it through the front
panel for the desired dips and dropouts. 
There are some models that are computer attached (RS232 or IEEE488) and you
execute software programmed routines for the test.

Mitigation?  Most EUT's can easily withstand half and single cycle drop,
many can take a little more (up to 5 cycles) before going seriously anemic.
Same is true for sags if the mains are wide range input.  If you fail, you
reselect the product's power supply, or beef up the input bulk capacitance
(assuming SMPS type) or adjust the monitoring circuitry (i.e. remote sense,
power good signal) for slower response and/or higher threshold.

For the -4-5 (surge) test; 
We use a schaffner NSG 650 attached to a pc running the schaffner surge
software.  The surges are delivered to the EUT through a CDN 110 coupler.
The cross coupling changes are manual jumpers.

We also have a Haefely Psurge 4010 and 32.1 coupling filter for heavy loads.
The cross coupling changes are automatic. 
The EUT supply cord length has to be no longer than .8M to the surge
generator. make a custom cable 
This test series can damage your EUT, so you might want to do this test
last. 
Mitigation of failures takes on a myriad of possibilities.  Wiring length,
TVSS absorber capacity, etc.  It is hard to say without knowing more about
your product.

Do you also need to do the -4-4 (EFT) test? 

All this test gear is large and heavy, particularly the power sources and
stepping xformers. 

Perhaps someone else can elucidate on exceptions to Class A rules? 

I gotta go, 
Happy Hunting, 
Kyle Ehler  KCØIQE 
 mailto:kyle.eh...@lsil.com mailto:kyle.eh...@lsil.com  
Assistant Design Engineer 
LSI Logic Storage Systems Div. 
3718 N. Rock Road 
U.S.A.  Wichita, Kansas  67226 
Ph. 316 636 8657 
Fax 316 636 8321 




-Original Message- 
From: wmf...@aol.com [ mailto:wmf...@aol.com mailto:wmf...@aol.com ] 
Sent: Monday, November 19, 2001 10:29 AM 
To: emc-p...@ieee.org 
Subject: Methods  Equipment; Surge  Dips 



Esteemed listmembers, 

In gearing-up for testing under the auspices of EN61326:97, I'm trying to
understand two immunity tests: EN61000-4-5 (surge immy) and -4-11 (dips
immy). Is there test equipment one can rent to conduct these tests? What
sort of mitigation steps are typical. Is anyone aware of any exceptions for
this testing under ClassA rules?

Thanks in advance... 
Wm Flanigan 
Standards Engineer 
Ameritherm Inc 



RE: Methods Equipment; Surge Dips

2001-11-20 Thread Ehler, Kyle
True, but did KT have this equipment 4yrs ago?
Does anyone you know of rent this equipment?
 
We also have a Schaffner tap switcher, but it eats itself under heavy loads.
Is the KT stuff more robust under heavy startup loads?
The Pacific Power equipment I use has never broke down.  Worth the weight
just for that...
kyle

-Original Message-
From: Mike Hopkins [mailto:mhopk...@thermokeytek.com]
Sent: Tuesday, November 20, 2001 2:47 PM
To: 'Ehler, Kyle'; 'wmf...@aol.com'; emc-p...@ieee.org
Subject: RE: Methods  Equipment; Surge  Dips


Seems to me this is the hard way to do it. 
KeyTek has a product that is a tap switcher for the required levels and will
pass the in-rush currents required. It's a much smaller package.
 
Also, other manufacturers have systems that are basically software
controlled switches -- bring in the AC levels you require via a variac or
some other transformer and simply switch between them
 
Mike Hopkins

-Original Message-
From: Ehler, Kyle [mailto:keh...@lsil.com]
Sent: Tuesday, November 20, 2001 1:19 PM
To: 'wmf...@aol.com'; emc-p...@ieee.org
Subject: RE: Methods  Equipment; Surge  Dips



Hi William, 
I dont know about renting equipment for the tests. 
You can probably find it. 

For the -4-11 (dip/dropout) test; 
Depending on your load, your site wiring has to be up to snuff. 
The power sources for doing the dip and dropout test are hefty stuff. 
My lab uses a three-phase powered source to deliver a max of 16A into a
single phase capacitive (SMPS) load. 
I have a Pacific Power 140 TMX and an AMX 390.  The 140 does
flicker/harmonics and can do dip/dropout within its output limits (about 10A
inrush).  Any loads beyond a 10A inrush gets dip/dropout tested by the 390.
The 140 is totally pc controlled but can be programmed through the front
panel.  It is a handy doer.

The 390 is the heavy (up to 20A inrush) and I program it through the front
panel for the desired dips and dropouts. 
There are some models that are computer attached (RS232 or IEEE488) and you
execute software programmed routines for the test.

Mitigation?  Most EUT's can easily withstand half and single cycle drop,
many can take a little more (up to 5 cycles) before going seriously anemic.
Same is true for sags if the mains are wide range input.  If you fail, you
reselect the product's power supply, or beef up the input bulk capacitance
(assuming SMPS type) or adjust the monitoring circuitry (i.e. remote sense,
power good signal) for slower response and/or higher threshold.

For the -4-5 (surge) test; 
We use a schaffner NSG 650 attached to a pc running the schaffner surge
software.  The surges are delivered to the EUT through a CDN 110 coupler.
The cross coupling changes are manual jumpers.

We also have a Haefely Psurge 4010 and 32.1 coupling filter for heavy loads.
The cross coupling changes are automatic. 
The EUT supply cord length has to be no longer than .8M to the surge
generator. make a custom cable 
This test series can damage your EUT, so you might want to do this test
last. 
Mitigation of failures takes on a myriad of possibilities.  Wiring length,
TVSS absorber capacity, etc.  It is hard to say without knowing more about
your product.

Do you also need to do the -4-4 (EFT) test? 

All this test gear is large and heavy, particularly the power sources and
stepping xformers. 

Perhaps someone else can elucidate on exceptions to Class A rules? 

I gotta go, 
Happy Hunting, 
Kyle Ehler  KCØIQE 
 mailto:kyle.eh...@lsil.com mailto:kyle.eh...@lsil.com  
Assistant Design Engineer 
LSI Logic Storage Systems Div. 
3718 N. Rock Road 
U.S.A.  Wichita, Kansas  67226 
Ph. 316 636 8657 
Fax 316 636 8321 




-Original Message- 
From: wmf...@aol.com [ mailto:wmf...@aol.com mailto:wmf...@aol.com ] 
Sent: Monday, November 19, 2001 10:29 AM 
To: emc-p...@ieee.org 
Subject: Methods  Equipment; Surge  Dips 



Esteemed listmembers, 

In gearing-up for testing under the auspices of EN61326:97, I'm trying to
understand two immunity tests: EN61000-4-5 (surge immy) and -4-11 (dips
immy). Is there test equipment one can rent to conduct these tests? What
sort of mitigation steps are typical. Is anyone aware of any exceptions for
this testing under ClassA rules?

Thanks in advance... 
Wm Flanigan 
Standards Engineer 
Ameritherm Inc 


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Technical Committee emc-pstc discussion list. 

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All 

RE: Methods Equipment; Surge Dips

2001-11-20 Thread Mike Hopkins
Seems to me this is the hard way to do it. 
KeyTek has a product that is a tap switcher for the required levels and will
pass the in-rush currents required. It's a much smaller package.
 
Also, other manufacturers have systems that are basically software
controlled switches -- bring in the AC levels you require via a variac or
some other transformer and simply switch between them
 
Mike Hopkins

-Original Message-
From: Ehler, Kyle [mailto:keh...@lsil.com]
Sent: Tuesday, November 20, 2001 1:19 PM
To: 'wmf...@aol.com'; emc-p...@ieee.org
Subject: RE: Methods  Equipment; Surge  Dips



Hi William, 
I dont know about renting equipment for the tests. 
You can probably find it. 

For the -4-11 (dip/dropout) test; 
Depending on your load, your site wiring has to be up to snuff. 
The power sources for doing the dip and dropout test are hefty stuff. 
My lab uses a three-phase powered source to deliver a max of 16A into a
single phase capacitive (SMPS) load. 
I have a Pacific Power 140 TMX and an AMX 390.  The 140 does
flicker/harmonics and can do dip/dropout within its output limits (about 10A
inrush).  Any loads beyond a 10A inrush gets dip/dropout tested by the 390.
The 140 is totally pc controlled but can be programmed through the front
panel.  It is a handy doer.

The 390 is the heavy (up to 20A inrush) and I program it through the front
panel for the desired dips and dropouts. 
There are some models that are computer attached (RS232 or IEEE488) and you
execute software programmed routines for the test.

Mitigation?  Most EUT's can easily withstand half and single cycle drop,
many can take a little more (up to 5 cycles) before going seriously anemic.
Same is true for sags if the mains are wide range input.  If you fail, you
reselect the product's power supply, or beef up the input bulk capacitance
(assuming SMPS type) or adjust the monitoring circuitry (i.e. remote sense,
power good signal) for slower response and/or higher threshold.

For the -4-5 (surge) test; 
We use a schaffner NSG 650 attached to a pc running the schaffner surge
software.  The surges are delivered to the EUT through a CDN 110 coupler.
The cross coupling changes are manual jumpers.

We also have a Haefely Psurge 4010 and 32.1 coupling filter for heavy loads.
The cross coupling changes are automatic. 
The EUT supply cord length has to be no longer than .8M to the surge
generator. make a custom cable 
This test series can damage your EUT, so you might want to do this test
last. 
Mitigation of failures takes on a myriad of possibilities.  Wiring length,
TVSS absorber capacity, etc.  It is hard to say without knowing more about
your product.

Do you also need to do the -4-4 (EFT) test? 

All this test gear is large and heavy, particularly the power sources and
stepping xformers. 

Perhaps someone else can elucidate on exceptions to Class A rules? 

I gotta go, 
Happy Hunting, 
Kyle Ehler  KCØIQE 
 mailto:kyle.eh...@lsil.com mailto:kyle.eh...@lsil.com  
Assistant Design Engineer 
LSI Logic Storage Systems Div. 
3718 N. Rock Road 
U.S.A.  Wichita, Kansas  67226 
Ph. 316 636 8657 
Fax 316 636 8321 




-Original Message- 
From: wmf...@aol.com [ mailto:wmf...@aol.com mailto:wmf...@aol.com ] 
Sent: Monday, November 19, 2001 10:29 AM 
To: emc-p...@ieee.org 
Subject: Methods  Equipment; Surge  Dips 



Esteemed listmembers, 

In gearing-up for testing under the auspices of EN61326:97, I'm trying to
understand two immunity tests: EN61000-4-5 (surge immy) and -4-11 (dips
immy). Is there test equipment one can rent to conduct these tests? What
sort of mitigation steps are typical. Is anyone aware of any exceptions for
this testing under ClassA rules?

Thanks in advance... 
Wm Flanigan 
Standards Engineer 
Ameritherm Inc 


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Administrative message -- Decorum

2001-11-20 Thread Rich Nute




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RE: Define Continuous DC Voltage - defibrillation

2001-11-20 Thread Bill Owsley


At 12:56 PM 11/20/2001 , Gary McInturff wrote:
urn:schemas-microsoft-com:office:office
xmlns:w = urn:schemas-microsoft-com:office:word xmlns:st1 =
urn:schemas-microsoft-com:office:smarttags 
Robert,

Thanks for this very
interesting piece of data. I've often wonder what atrioventricular
fibrillation is, you provide some insight on that as well.

If it is a reset of
sorts then how did the thumping of the chest ever work? I suppose it can
also fall into the category of just being better than nothing at all.

I have learned the chest thump, the pre-cordial thump, is for
witnessed events.
ex: Why doesn't CPR teach the pre-cordial
thump?
The pre-cordial thump is a technique that
involves a firm blow to the chest above the heart using a closed 'fist'.
This method is only taught in particular settings, for example the
electrical industry and it is recommended that the pre-cordial thump only
be administered in the event of an arrest witnessed by an individual
trained in the procedure. Furthermore, ARC guidelines recommend that the
pre-cordial thump is not a technique suitable for laypeople to be trained
in or to administer.
http://www.cpr2000.qas.qld.gov.au/faq/
or
MEF influences
pacemaker rate, causes diastolic depolarisation, and affects action
potential repolarisation. It contributes to the positive chronotropic
response of the heart to stretch, transient-stretch induced ectopic
excitation (including sudden cardiac death after moderate precordial
impact - Commotio cordis) and arrhythmogenesis in pressure or
volume overloaded hearts. On the other hand, if used appropriately,
pre-cordial impact can be a highly efficient means of mechanical
pacemaking and cardioversion. Mechanisms of cardiac MEF include
stretch-activation of ion channels, mechanical modulation of
Ca2+
handling, and interaction with mechano-sensitive non-myocytes of the
heart. We study these mechanisms in isolated cardiac cells, cell pairs,
culture and tissue. Methods include the single and double whole cell
patch clamp techniques, fluorescence microscopy, and optical mapping
(currently under development). Interventions involve axial stretch of
isolated cells, swelling, local membrane deformation, pharmacological
block of ion channels, etc. As part of Professor Denis Noble’s
BHF
Chair for Cardiovascular
Physiology we also
make extensive use of mathematical modelling for data interpretation,
hypothesis formation and design of experimental protocols.
http://www.physiol.ox.ac.uk/Graduate_Studies/Research_Interests/kohl2000.html

It is related to the rare newspaper article of someone getting hit
in the chest with a ball and dropping dead. Speculation has it that
the timing was un-lucky and hit at the moment that the heart timing could
be stopped. The pre-cordial thump is the reverse. EMT's in
this state are not taught the technique.

- Bill



I can be
learned wrong and always look for a better understanding. Its
been awhile but I believe the information came from one of the product
safety seminars in the Seattle (Rich N. I'm staring pretty hard at you
for the moment) area and I don't know really remember the speaker, but it
made a great deal of sense to me at the time and obviously most of it
stuck with me. (You'll notice I am not taking any blame even if my
information is wrong)

Thanks

Gary



-Original Message-
From: robertj
[mailto:robe...@ma.ultranet.com]
Sent: Tuesday, November 20, 2001 9:12 AM
To: 'Bill Owsley'; 'Gary McInturff'; 'Gregg Kervill'; 'Rich
Nute'
Cc: jrbar...@lexmark.com; emc-p...@majordomo.ieee.org
Subject: RE: Define Continuous DC Voltage - defibrillation


I also have not encountered the theory about chest compression
controlling fibrillation. Since defibrillation is also controlled during
open heart surgery by paddles directly applied to the heart and through
the use of wire catheters from implantable defibrillators, it is not the
only means.
I thought it might be interesting to describe the heart function in
electrical terms since that is the basis of understanding for most of us
in this group.

Heart muscle can be viewed as a simple free running flip-flop
oscillator. When cut into pieces, each piece of heart muscle will
automatically fire (contract) at its own natural rate. It can be
triggered earlier by input from neighboring tissue. Once it fires, it
goes through a relaxation stage when it is quite resistant to triggering
by neighboring tissue. This firing at a cellular level is call
depolarization. It is caused by the cell wall suddenly becoming permeable
to sodium and potassium ions and loosing its charge (which of course is a
current flow). The cell then takes time to recharge by pumping ions back
across the cell wall.

The master clock for the heart is the sinoatrial (SA) node (the sinus
node mentioned by Gary). This node sets the pace for the heart in
response to assorted hormone and brain inputs. It is located in the right
atrium. Remember the heart has four chambers. The right atrium is a
collecting spot 

RE: Methods Equipment; Surge Dips

2001-11-20 Thread Ehler, Kyle
Hi William,
I dont know about renting equipment for the tests.
You can probably find it.

For the -4-11 (dip/dropout) test;
Depending on your load, your site wiring has to be up to snuff.
The power sources for doing the dip and dropout test are hefty stuff.
My lab uses a three-phase powered source to deliver a max of 16A into a
single phase capacitive (SMPS) load.
I have a Pacific Power 140 TMX and an AMX 390.  The 140 does
flicker/harmonics and can do dip/dropout within its output limits (about 10A
inrush).  Any loads beyond a 10A inrush gets dip/dropout tested by the 390.
The 140 is totally pc controlled but can be programmed through the front
panel.  It is a handy doer.
The 390 is the heavy (up to 20A inrush) and I program it through the front
panel for the desired dips and dropouts.
There are some models that are computer attached (RS232 or IEEE488) and you
execute software programmed routines for the test.

Mitigation?  Most EUT's can easily withstand half and single cycle drop,
many can take a little more (up to 5 cycles) before going seriously anemic.
Same is true for sags if the mains are wide range input.  If you fail, you
reselect the product's power supply, or beef up the input bulk capacitance
(assuming SMPS type) or adjust the monitoring circuitry (i.e. remote sense,
power good signal) for slower response and/or higher threshold.

For the -4-5 (surge) test;
We use a schaffner NSG 650 attached to a pc running the schaffner surge
software.  The surges are delivered to the EUT through a CDN 110 coupler.
The cross coupling changes are manual jumpers.
We also have a Haefely Psurge 4010 and 32.1 coupling filter for heavy loads.
The cross coupling changes are automatic.
The EUT supply cord length has to be no longer than .8M to the surge
generator. make a custom cable
This test series can damage your EUT, so you might want to do this test
last.
Mitigation of failures takes on a myriad of possibilities.  Wiring length,
TVSS absorber capacity, etc.  It is hard to say without knowing more about
your product.

Do you also need to do the -4-4 (EFT) test?

All this test gear is large and heavy, particularly the power sources and
stepping xformers.

Perhaps someone else can elucidate on exceptions to Class A rules?

I gotta go,
Happy Hunting,
Kyle Ehler  KCØIQE
mailto:kyle.eh...@lsil.com 
Assistant Design Engineer
LSI Logic Storage Systems Div.
3718 N. Rock Road
U.S.A.  Wichita, Kansas  67226
Ph. 316 636 8657
Fax 316 636 8321




-Original Message-
From: wmf...@aol.com [mailto:wmf...@aol.com]
Sent: Monday, November 19, 2001 10:29 AM
To: emc-p...@ieee.org
Subject: Methods  Equipment; Surge  Dips



Esteemed listmembers,

In gearing-up for testing under the auspices of EN61326:97, I'm trying to
understand two immunity tests: EN61000-4-5 (surge immy) and -4-11 (dips
immy). Is there test equipment one can rent to conduct these tests? What
sort of mitigation steps are typical. Is anyone aware of any exceptions for
this testing under ClassA rules?

Thanks in advance... 
Wm Flanigan
Standards Engineer
Ameritherm Inc


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RE: Methods Equipment; Surge Dips

2001-11-20 Thread Chris Maxwell

Hi all,

John Crabb asked me about my previous response (see below).  He brings
up some points that I don't have experience with.  I wasn't sure how to
answer it.  I was hoping that someone else could address his concern.

For our AC powered equipment, we have never needed to add varistors,
MOV's, sidactors, TVS's ... to the AC mains for surge protection.  The
existing input filter (which carries its own safety approvals) has been
sufficient.So... I have never run into the component restriction
that John points out below.  If anybody else has, maybe they could
address John's question better than I?

However, we have used Sidactors, TVSs and/or MOVs on signal lines and
Telecom lines with good results.   The only major problems that we have
had are due to mismatch between power dissipation specs for a fuse and
MOV in a telecom circuit.  There were some instances where the MOV would
burn before the fuse would blow during power cross testing.

Chris

 -Original Message-
 From: Crabb, John [SMTP:jo...@exchange.scotland.ncr.com]
 Sent: Tuesday, November 20, 2001 12:13 PM
 To:   Chris Maxwell
 Subject:  RE: Methods  Equipment; Surge  Dips
 
 Chris, we have been considering using Harris (Littelfuse) 
 LA series varistors to overcome a surge problem, but it is 
 being highlighted to us that there is a CENELEC 
 OSM Decision that several European countries do not 
 accept the use of varistors between the mains and the 
 protective earth.
 
 Have you ever come across this restriction, and if so, how
 did you get round it ?
 (I gather UL and CSA have no such concerns).
 
 Regards,
 John Crabb, Development Excellence (Product Safety) , 
 NCR  Financial Solutions Group Ltd.,  Kingsway West, Dundee, Scotland.
 DD2
 3XX
 E-Mail :john.cr...@scotland.ncr.com
 Tel: +44 (0)1382-592289  (direct ). Fax +44 (0)1382-622243.
 VoicePlus
 6-341-2289.

---
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RE: Define Continuous DC Voltage - defibrillation

2001-11-20 Thread Gary McInturff
Robert,
Thanks for this very interesting piece of data. I've often wonder what
atrioventricular fibrillation is, you provide some insight on that as well.
If it is a reset of sorts then how did the thumping of the chest ever
work? I suppose it can also fall into the category of just being better than
nothing at all. 
I can be learned wrong and always look for a better understanding. Its
been awhile but I believe the information came from one of the product
safety seminars in the Seattle (Rich N. I'm staring pretty hard at you for
the moment) area and I don't know really remember the speaker, but it made a
great deal of sense to me at the time and obviously most of it stuck with
me. (You'll notice I am not taking any blame even if my information is
wrong)
Thanks
Gary

-Original Message-
From: robertj [mailto:robe...@ma.ultranet.com]
Sent: Tuesday, November 20, 2001 9:12 AM
To: 'Bill Owsley'; 'Gary McInturff'; 'Gregg Kervill'; 'Rich Nute'
Cc: jrbar...@lexmark.com; emc-p...@majordomo.ieee.org
Subject: RE: Define Continuous DC Voltage - defibrillation


I also have not encountered the theory about chest compression controlling
fibrillation. Since defibrillation is also controlled during open heart
surgery by paddles directly applied to the heart and through the use of wire
catheters from implantable defibrillators, it is not the only means.
I thought it might be interesting to describe the heart function in
electrical terms since that is the basis of understanding for most of us in
this group.
 
Heart muscle can be viewed as a simple free running flip-flop oscillator.
When cut into pieces, each piece of heart muscle will automatically fire
(contract) at its own natural rate. It can be triggered earlier by input
from neighboring tissue. Once it fires, it goes through a relaxation stage
when it is quite resistant to triggering by neighboring tissue. This firing
at a cellular level is call depolarization. It is caused by the cell wall
suddenly becoming permeable to sodium and potassium ions and loosing its
charge (which of course is a current flow). The cell then takes time to
recharge by pumping ions back across the cell wall.
 
The master clock for the heart is the sinoatrial (SA) node (the sinus node
mentioned by Gary). This node sets the pace for the heart in response to
assorted hormone and brain inputs. It is located in the right atrium.
Remember the heart has four chambers. The right atrium is a collecting spot
for the returning blood and when it contracts, moves the blood next door to
the right ventricle. The right ventricle pumps into the lungs. The left
atrium holds returning oxygenated blood and pushes it into the left
ventricle which pumps into the rest of the body. Obviously the ventricles
are the workhorses.
 
When the sinoatrial node fires, a wave of depolarization spreads over both
atria (1/10 of a second), but is protected from reaching the ventricles by a
layer of insulation. At the base of the right atrium it reaches the
atrioventricular (AV) node. This is a delay line (another 1/10 of a second)
and passes the signal to the left and right bundle branches which are
special conductors to get the signal quickly to all parts of the ventricles.
The AV delay provides the time for the atria to finish filling the
ventricles before the much more significant contraction of the ventricles.
 
Since all these conductors are live tissues, injury or irritation, depending
on where it occurs, can cause all sorts of problems like fast or slow
rhythms, lack of coordination of atria and ventricles, etc. One solution is
implantable pacemakers which in their simplest forms electrically trigger
the ventricles (the atria are left to themselves since they are not as
important).
 
Fibrillation occurs when something (like electric shock or irritation)
triggers a piece of heart muscle. This in turn triggers neighboring cells.
Unfortunately when the coordinated signal arrives from elsewhere, the cells
which have just fired can't respond since they have not gone through their
refractory period. These misfired cells then wait (while other parts are
recovering) and having waited too long, fire on their own again. When
several locations of the heart are doing this, the heart just quivers
instead of making a coordinated pumping effort. The fix is to provide an
electrical jolt which doesn't bother with triggering, it just hits all the
cells with enough energy to force depolarization anyway. Then all cells
together go through their refractory period and are ready for a coordinated
trigger (if it still exists). This is why very high shock levels can avoid
causing fibrillation.
 
Defibrillators have come a long way from the old days when they just applied
a severe 60 cycle AC shock. These days they try to provide a minimal level
impulse coordinated with any residual heart beat to force the heart into
unified action. The impulse can be applied with external paddles, and now is
available as a built in 

RE: Define Continuous DC Voltage - defibrillation

2001-11-20 Thread Bill Owsley


excellent - now if you'll go through the PQRST complex
also...

- Bill

At 12:11 PM 11/20/2001 , robertj wrote:

I
also have not encountered the theory about chest compression controlling
fibrillation. Since defibrillation is also controlled during open heart
surgery by paddles directly applied to the heart and through the use of
wire catheters from implantable defibrillators, it is not the only
means.

I thought it might be interesting to describe the heart function in
electrical terms since that is the basis of understanding for most of us
in this group.



Heart muscle can be viewed as a simple free running flip-flop oscillator.
When cut into pieces, each piece of heart muscle will automatically fire
(contract) at its own natural rate. It can be triggered earlier by input
from neighboring tissue. Once it fires, it goes through a relaxation
stage when it is quite resistant to triggering by neighboring tissue.
This firing at a cellular level is call depolarization. It is caused by
the cell wall suddenly becoming permeable to sodium and potassium ions
and loosing its charge (which of course is a current flow). The cell then
takes time to recharge by pumping ions back across the cell wall.



The master clock for the heart is the sinoatrial (SA) node (the sinus
node mentioned by Gary). This node sets the pace for the heart in
response to assorted hormone and brain inputs. It is located in the right
atrium. Remember the heart has four chambers. The right atrium is a
collecting spot for the returning blood and when it contracts, moves the
blood next door to the right ventricle. The right ventricle pumps into
the lungs. The left atrium holds returning oxygenated blood and pushes it
into the left ventricle which pumps into the rest of the body. Obviously
the ventricles are the workhorses.



When the sinoatrial node fires, a wave of depolarization spreads over
both atria (1/10 of a second), but is protected from reaching the
ventricles by a layer of insulation. At the base of the right atrium it
reaches the atrioventricular (AV) node. This is a delay line (another
1/10 of a second) and passes the signal to the left and right bundle
branches which are special conductors to get the signal quickly to all
parts of the ventricles. The AV delay provides the time for the atria to
finish filling the ventricles before the much more significant
contraction of the ventricles.



Since all these conductors are live tissues, injury or irritation,
depending on where it occurs, can cause all sorts of problems like fast
or slow rhythms, lack of coordination of atria and ventricles, etc. One
solution is implantable pacemakers which in their simplest forms
electrically trigger the ventricles (the atria are left to themselves
since they are not as important).



Fibrillation occurs when something (like electric shock or irritation)
triggers a piece of heart muscle. This in turn triggers neighboring
cells. Unfortunately when the coordinated signal arrives from elsewhere,
the cells which have just fired can t respond since they have not gone
through their refractory period. These misfired cells then wait (while
other parts are recovering) and having waited too long, fire on their own
again. When several locations of the heart are doing this, the heart just
quivers instead of making a coordinated pumping effort. The fix is to
provide an electrical jolt which doesn t bother with triggering, it just
hits all the cells with enough energy to force depolarization anyway.
Then all cells together go through their refractory period and are ready
for a coordinated trigger (if it still exists). This is why very high
shock levels can avoid causing fibrillation.



Defibrillators have come a long way from the old days when they just
applied a severe 60 cycle AC shock. These days they try to provide a
minimal level impulse coordinated with any residual heart beat to force
the heart into unified action. The impulse can be applied with external
paddles, and now is available as a built in part of implanted pacemakers
so the impulse can be applied directly to the heart using the pacing
electrodes.



Bob Johnson



-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]
On Behalf Of Bill Owsley
Sent: Monday, November 19, 2001 1:22 PM
To: Gary McInturff; 'Gregg Kervill'; 'Rich Nute'
Cc: jrbar...@lexmark.com; emc-p...@majordomo.ieee.org
Subject: RE: Define Continuous DC Voltage



I've never seen cardiac function or resuscitation explained this
way... and I'm an EMT-D. The D is for defibrillator and the
EMT is for emergency medical technician. And with very few
exceptions, the rest of the medical aspects of this discussion have been
suspect.
As my kids say - don't go there...

- Bill


At 12:02 PM 11/19/2001 , Gary McInturff wrote:


From a few
courses several years back.
The heart
has something called the Sinus node (spelling could be
wrong) The responsibility of that node is to control the 

RE: Quality Assurance and product approvals

2001-11-20 Thread Ehler, Kyle
You are all making some excellent points.
It would seem that many of us share commonality.  Perhaps that is one of the
underlying purposes of the quality organizations.  When followed, the
effects are positive and things move correctly, and in synch, but when
exceptions are present...
In my case, the compliance group and the engineering group are one.  This
obviously has good and bad implications.
 
Brian makes an excellent point that has at times caused my hackles to raise
more than once...the independence (or lack thereof) between the compliance
department and the engineering department.  In the company documents filed
by two of these quality agencies, i.e.  ISO 900x, A2LA, TUV or COMPASS,
there is a clause that specifically mentions the requirement for this
independence.  Or, is it more of a 'suggestion'?
 
There does not however, seem to be an audit check for departmental
independence.  I recently have become an ISO auditor, and I am uncertain
there is, UNLESS I want to take it upon myself to press the issue.  Since I
work in the department, I cannot be assigned the task of auditing it, but I
could express my concerns with the person assigned the audit of the
EMC/Safety/Design engineering department.  Hmm...
 
I dont recall where these clauses are, but the purpose behind them is to
express the importance of functional isolation between the interests of the
two groups.  In our case, this causes a disastrous effect on scheduling and
allocation of resources because the conflicts are quick to rise and there is
a weak attempt to resist.  At times, we find ourselves pulled in two
directions simultaneously.  The 'Janus'..?
 
All the planning, procedures and methods in the world cannot overcome this
conflict if no one is willing to meet the challenge and push the issue.
(as in our case)  My poor boss has been subdued...and our compliance group
is eternaly the whipping boy.  I see the problem, but I am ineffective at
fighting off the 800Lb gorilla's because they do not believe a lab
rat...could read, think and speak.  Ah, but I can AUDIT, or cause focus by
another auditor...that would attract the attention of the QA folks (who seem
to be beyond reproach).
 
In the end, the quality of our output is in the hands of the lab rats who,
take it upon themselves to ensure the letter of the standards are adhered to
despite the conflict associated with the work.  That makes it a thankless
job, with little if any, appreciation.  Ha!! what's that you say...you want
a medal?  -for driving up COSTS and delaying product release!!!  If it
were'nt for the beaurocracy...you would not have a job.

[Ehler, Kyle] 
(my words)
 
 -Original Message-
From: Brian McAuliffe [mailto:bally...@iolfree.ie]
Sent: Tuesday, November 20, 2001 4:36 AM
To: 'EMC-PSTC Discussion Group'
Subject: RE: Quality Assurance and product approvals



I think the point raised by Gary re: where the Compliance group fits into
the organisation structure is more important than procedures/process,
although I disagree with him about where that should be. Let me explain. 
 
Having a good working relationship with Engineering is indeed critical,
however from my experience I believe it essential for the Compliance group
to be organisationally independent of Engineering. If not, then there are
always conflicts of interest when allocating the (usually limited)
Compliance resources between:
 
Engineering - there are 4 design reviews this week and preparation required
for a safety pre-compliance test next week;
Operations  - the agency auditor is visiting next week and there is some
prep needed;
Sales/Marketing - the Russian approval is expiring in 2 weeks and you need
to re-apply, prepare doc pack, 
etc.
 
How do you prioritise without getting slack from at least one functional
head ?? Obviously if the Compliance group is actually a group and not just 1
or 2 persons, then with a good understanding of the roles amongst the group
members the above does not really pose a problem. However I do NOT believe
this is the case, particularly in the current climate of lay-offs, with us
Compliance folk are becoming less essential.
 
Unless the role of the Compliance group is very narrow and involves only
support of one function (which I doubt), I feel that an independent
Compliance group is essential. It should be functionally independent to any
other group and reporting to the MD, or, reporting to the QA
Director/Manager. This will mean you can realistically argue for adequate
resouces to do a professional job for all those groups requiring your
services. You will have somebody independent at the right level in the
organisation supporting the Compliance group - essential when $$$ are
involved. Let's face it, no RD Manager is going to approve headcount for a
2nd Compliance Engineer whose primary function is to do audits of the
production facility to ensure critical components are controlled as they
should, and, to support Sales/Marketing to achieve product approvals

RE: Define Continuous DC Voltage - defibrillation

2001-11-20 Thread robertj
I also have not encountered the theory about chest compression
controlling fibrillation. Since defibrillation is also controlled during
open heart surgery by paddles directly applied to the heart and through
the use of wire catheters from implantable defibrillators, it is not the
only means.
I thought it might be interesting to describe the heart function in
electrical terms since that is the basis of understanding for most of us
in this group.
 
Heart muscle can be viewed as a simple free running flip-flop
oscillator. When cut into pieces, each piece of heart muscle will
automatically fire (contract) at its own natural rate. It can be
triggered earlier by input from neighboring tissue. Once it fires, it
goes through a relaxation stage when it is quite resistant to triggering
by neighboring tissue. This firing at a cellular level is call
depolarization. It is caused by the cell wall suddenly becoming
permeable to sodium and potassium ions and loosing its charge (which of
course is a current flow). The cell then takes time to recharge by
pumping ions back across the cell wall.
 
The master clock for the heart is the sinoatrial (SA) node (the sinus
node mentioned by Gary). This node sets the pace for the heart in
response to assorted hormone and brain inputs. It is located in the
right atrium. Remember the heart has four chambers. The right atrium is
a collecting spot for the returning blood and when it contracts, moves
the blood next door to the right ventricle. The right ventricle pumps
into the lungs. The left atrium holds returning oxygenated blood and
pushes it into the left ventricle which pumps into the rest of the body.
Obviously the ventricles are the workhorses.
 
When the sinoatrial node fires, a wave of depolarization spreads over
both atria (1/10 of a second), but is protected from reaching the
ventricles by a layer of insulation. At the base of the right atrium it
reaches the atrioventricular (AV) node. This is a delay line (another
1/10 of a second) and passes the signal to the left and right bundle
branches which are special conductors to get the signal quickly to all
parts of the ventricles. The AV delay provides the time for the atria to
finish filling the ventricles before the much more significant
contraction of the ventricles.
 
Since all these conductors are live tissues, injury or irritation,
depending on where it occurs, can cause all sorts of problems like fast
or slow rhythms, lack of coordination of atria and ventricles, etc. One
solution is implantable pacemakers which in their simplest forms
electrically trigger the ventricles (the atria are left to themselves
since they are not as important).
 
Fibrillation occurs when something (like electric shock or irritation)
triggers a piece of heart muscle. This in turn triggers neighboring
cells. Unfortunately when the coordinated signal arrives from elsewhere,
the cells which have just fired can't respond since they have not gone
through their refractory period. These misfired cells then wait (while
other parts are recovering) and having waited too long, fire on their
own again. When several locations of the heart are doing this, the heart
just quivers instead of making a coordinated pumping effort. The fix is
to provide an electrical jolt which doesn't bother with triggering, it
just hits all the cells with enough energy to force depolarization
anyway. Then all cells together go through their refractory period and
are ready for a coordinated trigger (if it still exists). This is why
very high shock levels can avoid causing fibrillation.
 
Defibrillators have come a long way from the old days when they just
applied a severe 60 cycle AC shock. These days they try to provide a
minimal level impulse coordinated with any residual heart beat to force
the heart into unified action. The impulse can be applied with external
paddles, and now is available as a built in part of implanted pacemakers
so the impulse can be applied directly to the heart using the pacing
electrodes.
 
Bob Johnson
 
-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org] On Behalf Of Bill Owsley
Sent: Monday, November 19, 2001 1:22 PM
To: Gary McInturff; 'Gregg Kervill'; 'Rich Nute'
Cc: jrbar...@lexmark.com; emc-p...@majordomo.ieee.org
Subject: RE: Define Continuous DC Voltage
 
I've never seen cardiac function or resuscitation explained this way...
and I'm an EMT-D.  The D is for defibrillator and the EMT is for
emergency medical technician.  And with very few exceptions, the rest of
the medical aspects of this discussion have been suspect.
As my kids say - don't go there...

- Bill


At 12:02 PM 11/19/2001 , Gary McInturff wrote:



From a few courses several years back.
The heart has something called the Sinus node (spelling could be
wrong) The responsibility of that node is to control the timing of the
electric wave front if you will. The heart actually has about three
pulses. Looking at a heart 

EL (Electro Luminescent) considerations.

2001-11-20 Thread Enci

Hi Group, 

Could anyone tell me a little more about the safety implications/standards
for the use of EL wire/sheet. Specifically when powered from a battery
source,i.e. battery-inverter-EL, and the EL wire/sheet outer insulation
is exposed.

Thank you in advance,
Enci




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RE: Quality Assurance and product approvals

2001-11-20 Thread Gary McInturff
Morning Brian, et al.
I don't have a large heartburn about the exact organizational chart
location I have been in them all - well not actually sales I do have some
standards* - and I find the debate very valuable! 
Location doesn't really create or fix all that many problems. You kind
of trade one set of problems for the other. The absolute point of
criticality is that the corporation  has to have understand what it needs to
get a product to market. That is established in the products requirement
document, others may have different names. The things this group does,
including Safety, EMC, and NEBS, among others are quite simply product
requirements just like everything else in the document, in our case the
ability to pass packets at line rate without packet loss, or maybe
implementing spanning tree protocols etc. Take a look back at recent
discussions about whether or not a DOC by itself was sufficient to accept
product. The answer was generally no. That can affect a bottom line and that
always gets attention from the highest levels. Why? Because some of the
product features couldn't be independently verified and products aren't
being purchased without it. We just stopped purchases of some very expensive
pieces of equipment because of some operational bugs AND because of problems
with their radiated emissions. That affected that companies bottom line for
the quarter and that gets everybody's attention.
Once the feature issue is understood then things start falling into
place quite nicely. Making that understood is probably one of the more
critical items we have to face, and it can be done from any organization.
When the various prototype, pilot, or alpha builds are being planned they
include the units I need for my job - that will range from three to six
depending on the NEBS requirements, and these aren't inexpensive pieces of
equipment. Schedules are a sneaking little tool. When being laid out its not
a hard sale to point out that not having EUT's and having them on fixed
dates starts putting day to day slips into the production release of the
product. It also clearly identifies when more bodies are needed to implement
the schedule. Something the big guys can evaluate very effectively.
You're correct about the design review meetings and I spend a lot of
time either in them or responding via e-mail or cell phone to them. Its not
perfect but works very well. If I train the engineers well they become
somewhat self monitoring and learn to get quick verifications when they have
concerns. 
 Spokane is an absolutely wonderful place to live but it means that for
those tests I need to witness - EMC and  NEBS etc, I spend a great deal of
time in rectangular tubes at 30,000 feet trying to get to a rectangular box
at the end of the day - traveling is so much fun - but a laptop, a very
good electronic Engineering change process, a cell phone, and some first
rate engineers and lab rats and it works very well - again independent of
what organization I'm in. 
So get the features defined at step one, that will drive the
allocations, tasks and schedules. The work with some great people who
understand engineering and the full product development process - yes even
sales has its good points, but empire builders are expressly excluded, and
then work from anywhere. History has given me a strong preference for being
inside the engineering department but your choice is just as.
Gary

 
 
*(It was  a joke folks complain to me directly off line).  

-Original Message-
From: Brian McAuliffe [mailto:bally...@iolfree.ie]
Sent: Tuesday, November 20, 2001 2:36 AM
To: 'EMC-PSTC Discussion Group'
Subject: RE: Quality Assurance and product approvals


I think the point raised by Gary re: where the Compliance group fits into
the organisation structure is more important than procedures/process,
although I disagree with him about where that should be. Let me explain. 
 
Having a good working relationship with Engineering is indeed critical,
however from my experience I believe it essential for the Compliance group
to be organisationally independent of Engineering. If not, then there are
always conflicts of interest when allocating the (usually limited)
Compliance resources between:
 
Engineering - there are 4 design reviews this week and preparation required
for a safety pre-compliance test next week;
Operations  - the agency auditor is visiting next week and there is some
prep needed;
Sales/Marketing - the Russian approval is expiring in 2 weeks and you need
to re-apply, prepare doc pack, 
etc.
 
How do you prioritise without getting slack from at least one functional
head ?? Obviously if the Compliance group is actually a group and not just 1
or 2 persons, then with a good understanding of the roles amongst the group
members the above does not really pose a problem. However I do NOT believe
this is the case, particularly in the current climate of lay-offs, with us
Compliance folk 

RE: 80/80 rule for euro compliance?

2001-11-20 Thread georgea



Actually, Vilfredo Pareto (1848-1923) was an Italian economist.
He observed that 80% of the economy was driven by 20% of the
consumers, i.e. 20% of the customers account for 80% of the
turnover.

Two decades ago I was involved in an effort to create a data bank
of IBM typewriter service customers.  Some customers (e.g. banks)
owned many units, and placed many calls for service, while fewer
calls came from individuals owning one machine.  It became evident
that 20% of the customers accounted for 80% of the service calls.
The data base was set up to maintain the phone numbers of only the
most active 20%, as this required 80% less computer space.  When a
call came in, the customer was asked for their phone number.  If it
was one of the 20%, the operator then saw a full screen of data as
to the name, address and service history of the customer, saving
time on the phone keying data.

It would probably be correct to say that 80% of the work is done
by 20% of the workers; however, it would still take 100% of effort
to complete 100% of the work.

George Alspaugh




Gregg Kervill gkervill%eu-link@interlock.lexmark.com on 11/14/2001
08:03:00 AM

Please respond to Gregg Kervill gkervill%eu-link@interlock.lexmark.com

To:   'Doug McKean' dmckean%corp.auspex@interlock.lexmark.com,
  'EMC-PSTC Discussion Group'
  emc-pstc%majordomo.ieee@interlock.lexmark.com
cc:(bcc: George Alspaugh/Lex/Lexmark)
Subject:  RE: 80/80 rule for euro compliance?




Liars, Damn Liars and .



I sounds like the Pareto's law from management statistics You can do 80% of
the work with 20% of the effort...



I think someone requoted it once as You an fool some of the people all of
the time.



Cynically yours  Gregg





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RE: Methods Equipment; Surge Dips

2001-11-20 Thread Chris Maxwell

Hi Wm (my guess is William),

Didn't see a response to your question.  Got lots to do today, so I'll
be quick and dirty.  (Well I thought I would...as you can see it wasn't
so quick but it is dirty :-)

Test equipment...

Surge Testing...
There are quite a few companies that make equipment that can test this.
Haefley, Compliance Design,  Schaffner and Keytek come to mind.  We use
a Keytek CE-Master.  It will handle most power line surge testing that
would be required.  However, it won't do the 10/700 waveforms for
telecom surge (unless they have a new unit or new module).   It also may
have trouble  surge testing signal lines and other non-power lines
unless you get the proper coupling/decoupling network.  

Dips  Interrupt (also known as Power Quality Failure (PQF) testing... 
Same manufacturers as above.  We use the CE-master for this test as
well.  (This is not a commercial for CE-master...it's just what we
have.) One caveat regarding dip and interrupt testing is that you need a
power source capable of high in-rush capacities to power the device
under test.  We use a typical wall outlet with a non-current limited
isolation transformer to make 230VAC.  If you use a current limited
110-230VAC converter, it may not be able to provide enough in-rush to
test fairly.  (check out the manual, it will explain)Oh yeah, I just
remembered.  Most of the standards say to test for 1 cycle of 50Hz.  The
CE-master will not generate 50Hz for you, instead it will only pass your
60Hz through it.  We get around this by testing for two cycles of 60Hz
instead of one cycle of 50Hz.  It's a worst case, and keeps us from
having to buy a 50Hz inverter (that isn't current limited...see above).

Mitigation techniques...

Surge.  Depends upon the surge level needed to pass and the sensitivity
of your equipment.  Protection could be provided by the typical EMC
filtering that you already have.  (i.e. a power line filter with caps
and chokes).  If the surge is too powerful for your existing filter, you
can either get a surge rated input filter or put a surge protection
device on (watchout for your leakage current specs for safety).  I
recommend either a TVS or Sidactor.  I used to worry about Sidactor
availability as they were only available in 2,500 piece quantities, but
are now available in small quantities from Digikey.  Some manufacturers:
TVS diodesSemtech, Protek   Sidactors... Teccor, Rachem Polyswitch.

Dips  Interrupts.
Main mitigation technique here is bulk capacitance to provide enough
hold-up time so that your equipment doesn't power down during a small
dip or interrupt.  If you are using a power supply in your design, check
out its hold-up time spec.  So far, from our experience it appears that
a supply with at least a 15milllisecond hold-up time will get you
through the test.

In rare instances, in-rush limiting may be required.  Probably not.

Exemptions?

Class A is an emissions classification under the standard (EN
61326-1).  Using Class A as an immunity classification may lead you
down the wrong path.  I would suggest considering immunity independently
of emissions and classifying the equipment for immunity as industrial
(annex A), controlled EM environments (annex B) or portable (annex
C).  Once you have picked the correct annex, the question to test or
not to test will be answered.  In order to determine the test level and
performance criterion, use the annex picked above and then refer to
Table 2 and classify your equipment as for essential operation,
continuous unmonitored operation, continuous monitored operation or
non-continuous operation.

There is also a Table 1 which specifies an absolute minimum immunity
level for EN 61326-1 classified equipment.  I use this as a benchmark,
but usually test to higher levels as specified in the annexes.

I hope there was something useful in there for you.

Chris Maxwell | Design Engineer - Optical Division
email chris.maxw...@nettest.com | dir +1 315 266 5128 | fax +1 315 797
8024

NetTest | 6 Rhoads Drive, Utica, NY 13502 | USA
web www.nettest.com | tel +1 315 797 4449 | 






 -Original Message-
 From: wmf...@aol.com [SMTP:wmf...@aol.com]
 Sent: Monday, November 19, 2001 11:29 AM
 To:   emc-p...@ieee.org
 Subject:  Methods  Equipment; Surge  Dips
 
 
 Esteemed listmembers,
 
 In gearing-up for testing under the auspices of EN61326:97, I'm trying
 to understand two immunity tests: EN61000-4-5 (surge immy) and -4-11
 (dips immy). Is there test equipment one can rent to conduct these
 tests? What sort of mitigation steps are typical. Is anyone aware of
 any exceptions for this testing under ClassA rules?
 
 Thanks in advance... 
 Wm Flanigan
 Standards Engineer
 Ameritherm Inc
 
 
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[Fwd: Student Design Contest from IEEE EMC Education Committee]

2001-11-20 Thread reheller

I'd like to pass this on to the group.

Bob Heller
3M Product Safety, 76-1-01
St. Paul, MN 55107-1208
Tel:  651- 778-6336
Fax:  651-778-6252

- Forwarded by Robert E. Heller/US-Corporate/3M/US on 11/20/2001 05:46
AM -

Greetings,


 Original Message 
Subject: Student Design Contest from IEEE EMC Education Committee
List-Post: emc-pstc@listserv.ieee.org
Date: Tue, 13 Nov 2001 14:44:26 -0600
From: Robert Nelson robert.m.nel...@ndsu.nodak.edu

Dear IEEE EMC Education Committee members (and interested folks),

The Education Committee of the IEEE EMC (Electromagnetic Compatibility)
Society is sponsoring the third annual EMC Student Design Competition, and
would like to invite students you know to enter.  In a nutshell
the contest involves registering to receive a noisy circuit (electrically
noisy, that is), and designing appropriate fixes to make the circuit
quieter.

Your students might win $900 plus a trip to the 2002 International
IEEE EMC Symposium to be held in Minneapolis, MN in August 2002!

Additional information about the contest is available either from the
home page for the IEEE EMC Society ( http://www.ewh.ieee.org/soc/emcs/ ),
(noting that there are two links dealing with the contest) or from
the home page for the Education Committee
( http://www.ewh.ieee.org/soc/emcs/edu/index.html ).  Please go to the link
discussing the Contest.  You might also want to peruse an article written
about the 2001 contest. This is available via the link on the page
  http://www.ewh.ieee.org/soc/emcs/edu/edurpts.htm

If you have any questions, please contact Ahmad Fallah (
ahmadfal...@ieee.org ).


Thanks for passing this on!

Sincerely,

Dr. Bob Nelson
Secretary, IEEE EMC Education Committee
North Dakota State University
Dept. of Electrical and Computer Eng.
Fargo, ND  58105
V: (701)-231-7619
F: (701)-231-8677
E-mail: r.m.nel...@ieee.org






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SV: Walkie-Talkie in Thailand

2001-11-20 Thread h . knudsen

Hello KC Chan,
In Thailand the bands 26.960 - 27.410 MHz, 77.9875 - 79 MHz and 244.9875 -
246 MHz are
designated as Citizens Band (CB). The bands 79 - 79.9875 MHz and 246 - 247
MHz are
reserved for similar purposes.

You may download the Thai frequency allocation table from
http://www.ptd.go.th/services_eng.htm
Links to this kind of information may often be found on the ITU page:
http://www7.itu.int/treg/profiles2/CntryPrfiles/guide.asp

Best regards

Helge Knudsen
Test  Approval manager
Niros Telecommunication
Hirsemarken 5
DK-3520 Farum
Denmark
Tel +45 44 34 22 51
Fax +45 44 99 28 08
email h.knud...@niros.com

-Oprindelig meddelelse-
Fra: KC CHAN [PDD] [mailto:kcc...@hkpc.org]
Sendt: 20. november 2001 08:13
Til: emc-p...@majordomo.ieee.org
Emne: Walkie-Talkie in Thailand



Hi

I got an enquiry about the walkie-talkie in Thailand.  Does anyone know the
frequency band for this purpose in Thailand, and where I can get more
information about this.

Thank You
KC Chan


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RE: Quality Assurance and product approvals

2001-11-20 Thread Brian McAuliffe
I think the point raised by Gary re: where the Compliance group fits into
the organisation structure is more important than procedures/process,
although I disagree with him about where that should be. Let me explain.

Having a good working relationship with Engineering is indeed critical,
however from my experience I believe it essential for the Compliance group
to be organisationally independent of Engineering. If not, then there are
always conflicts of interest when allocating the (usually limited)
Compliance resources between:

Engineering - there are 4 design reviews this week and preparation required
for a safety pre-compliance test next week;
Operations  - the agency auditor is visiting next week and there is some
prep needed;
Sales/Marketing - the Russian approval is expiring in 2 weeks and you need
to re-apply, prepare doc pack, 
etc.

How do you prioritise without getting slack from at least one functional
head ?? Obviously if the Compliance group is actually a group and not just 1
or 2 persons, then with a good understanding of the roles amongst the group
members the above does not really pose a problem. However I do NOT believe
this is the case, particularly in the current climate of lay-offs, with us
Compliance folk are becoming less essential.

Unless the role of the Compliance group is very narrow and involves only
support of one function (which I doubt), I feel that an independent
Compliance group is essential. It should be functionally independent to any
other group and reporting to the MD, or, reporting to the QA
Director/Manager. This will mean you can realistically argue for adequate
resouces to do a professional job for all those groups requiring your
services. You will have somebody independent at the right level in the
organisation supporting the Compliance group - essential when $$$ are
involved. Let's face it, no RD Manager is going to approve headcount for a
2nd Compliance Engineer whose primary function is to do audits of the
production facility to ensure critical components are controlled as they
should, and, to support Sales/Marketing to achieve product approvals
worldwide.

(To bring this back to procedures/process) There also needs to be a
'document' which highlights:

1. What services the Compliance group offer;
2. The inputs (from other groups) required, and the outputs to be expected
from each service;
3. Turnaround time (this will never be 100% accurate)

With a document such as this published it raises awareness among each of the
functions that the Compliance group do have organisation-wide
responsibilites and are not at the beck and call of just one group. It
forces them to plan for compliance also. It gives the Compliance group more
credibility and visibility, and maybe people will start to appreciate the
.

Brian
  -Original Message-
  From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Gary McInturff
  Sent: 19 November 2001 16:35
  To: 'Tania Grant'; am...@westin-emission.no; 'EMC-PSTC Discussion Group'
  Subject: RE: Quality Assurance and product approvals



  Bottom line is that each program generates a set of milestones that
identify a function, set of equipment required, and timeframe for getting
them done, and there are a set of generic test suites, but generally the
whole process is documented at very non-descript level. The rest of this is
rational for the way it happens.
  Over the course of my career ( companies of 40 - to 1,000 employees)
this function has 1) grown in scope, first just safety, then safety and EMC,
then safety, EMC and DVT, currently its safety, EMC, DVT, and NEBS. 2) It
has been shuffled from place to place. Engineering, QA, manufacturing, to
marketing. I have always been able to direct it back to what I believe is
the correct department - Engineering. Principally for, conservation of
resources - I already have some lab rats ( I say this with humor they have
saved me much time and grief over the years) , and equipment, I may have to
expand the equipment set marginally but I don't have to duplicate it.
Probably just as important, is that inside of engineering I have the most
timely input into the design changes or recommendations up front. Being
located with the design engineers gives us both immediate and personal
contact. They can stop into my office, and do quite regularly, to ask
questions or seek advice, and I can do the same.
  As for formality of process it has always been more a series of
milestones rather than explicitly documented processes for the vary reason
Tania states - things change and they can change rapidly. I do have a series
of boilerplate tests such as temperature, etc but occasionally those tests
end up confirming - not predicting - what the safety agencies find. I try to
find the very earliest point at which I can submit product to the safety
agencies and the product is not always 100% functional from a design
perspective, but 100% representative 

RE: John Woodgate Departure

2001-11-20 Thread Chris Chileshe

Dear all,

I guess I should have known better than to open a can of worms and then
have the audacity to take a day off!! I returned today ( Tuesday) to find my 
in-folder overflowing with opinions on this matter. 

It is quite obvious that John's presence is treasured by quite a large
percentage of the list.

However, there has been noticeable shift in the tone of the messages
addressing the issue in that there is some degree of casting the 
administrator as the villain of the peace here (contrary to the Hollywood
norm which always has the English guy as the villain!). This is neither 
right nor fair (I am not talking about Hollywood anymore although it wouldn't
do them any harm to take notes!!). It was certainly not the intention of my 
original posting and my appeal was to both John and the list admin. 

My apologies to the list administrator for this misunderstanding and unfortunate
change in ethos. 

I think it best we leave the matter to John and the administrator
to resolve.

To this end, Chris Maxwell writes ..

 If there is any peacemaking to be done here, I suggest that 
 John and the admin in question work it out off-line.  

Agreed. Chris adds...

 I suggest that if a third party get involved, that it also be off-line.  
 (I suggest Tania.  She'll straighten them out :-))  

So ... what are you saying Chris .. Kofi Annan not good enough for you?

But seriously, let us not point fingers and leave the gentlemen to work it 
out. The most we can do is appeal to John to reconsider HIS decision.

Best regards everyone.

- Chris

--
Don't you just love the swooshing sound deadlines make as they go
flying past!   

 

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Walkie-Talkie in Thailand

2001-11-20 Thread KC CHAN [PDD]

Hi

I got an enquiry about the walkie-talkie in Thailand.  Does anyone know the 
frequency band for this purpose in Thailand, and where I can get more 
information about this.

Thank You
KC Chan


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Re: Quality Assurance and product approvals

2001-11-20 Thread mike harris
Hi Tania,

I just finished writing a procedure on agency certifications for a client 
(prompted by their ISO 9000 audit). It became partly glossary  partly 
encyclopedia so sales, marketing, etc could find definitions and explanations 
of what the agencies are and why we need the certifications. It identifies the 
different levels  types of certifications  why they are needed by various 
parties. It outlines who does what, as far as design (initial  ongoing), 
purchasing (ongoing - no stealth changes of critical parts), parts/materials 
inventory (traceability), etc. It defines who gets notified of new 
certifications  what records are kept  for how long.

I agree with you completely that it would be never-ending to try to write a 
procedure to allow the untrained to do it all, so it does not explain how to 
conduct a project at any agency except in the most basic terms (tell the agency 
what you want to certify, get their cost estimate, write PO, provide samples  
documentation, assist as needed).

Much can be gained by having such a document, which will seem basic for any 
competent compliance engineer. It will so nice to refer people to the procedure 
for the routine questions, instead of doing Agency 101 for the umpteenth time.

Mike Harris/Teccom
-Original Message-
From: Tania Grant taniagr...@msn.com
To: am...@westin-emission.no am...@westin-emission.no; 'EMC-PSTC 
Discussion Group' emc-p...@majordomo.ieee.org
Date: Monday, November 19, 2001 1:18 AM
Subject: Re: Quality Assurance and product approvals


Amund,

Since I transferred, over more than 20 years ago, from Quality Assurance to 
Regulatory compliance/product safety, I will share with you my opinions and my 
experience.   However, I would also be interested in hearing about the 
experience of others.

In my opinion, QA and regulatory compliance are different enough functions 
that require different experiences and disciplines that would not necessarily 
make it effective for a QA organization to either write or enforce procedures 
on the regulatory compliance functions.  That does not mean that regulatory 
compliance shouldn't have a more formal process and a procedure to go with it.  
 For myself, I know that having a QA background made me a more effective 
regulatory guru at the company.  But I don't see how the two can be meshed 
under the same umbrella without diluting one or the other.  Both require focus 
but it would be a rare Janus that could manage this effectively.   

However, the regulatory processes could, and should, be integrated into the 
whole engineering design process;-- and so should the QA process.   Thus, the 
two can and should help each other, but I just don't see that a QA oversight by 
itself would make the regulatory process better or more effective.   

Now, I have a problem with your statement  ...have your companies made 
procedures which in details describes the product approval process from 
beginning to end ?   You are quite right that any procedure should describe a 
process in detail from beginning to end.   This lends itself quite well to any 
and all test procedures, assembly of various parts, and other such functions 
where the same process is repeated over and over again.   However, with the 
regulatory approval process, each product is different enough, that a 
procedure, especially one that is detailed, would not work.   And the 
approval process is not always from the beginning to end but very often just 
a test or two have to be repeated, but not all, and sometimes you just notify 
the authorities about this and that, and sometimes you don't, but only document 
it or write up a justification why a particular test is not required.   So how 
do you write a procedure around this?   If I had to religiously do all this, I 
would be writing a procedure practically every time I was submitting a new or 
providing changes to a product.   And I sure as heck would have been very upset 
if someone else (say from QA) were writing these procedures for me, 
especially since they wouldn't know what was required, or how to achieve this.  

A procedure describes how something is done.   If I don't know how to do 
it, I shouldn't be working in that position.   If the QA person is writing such 
a procedure (and assuming they are effective at it, which is problematic) then 
they should be working in that position and not me.   

Thus, I am not in favor of procedures.   However, I am very much in favor 
of regulatory compliance plans that should be written for each new product, or 
a major regulatory up-date to a product.   This compliance plan is really a 
communication device that informs Marketing, Engineering, QA, etc., the 
regulatory strategy: what the requirements are for this particular product, for 
which countries, to which standards, where the various tests will be performed, 
the approximate time assuming only one sample is