RE: EN 60601-1-2/ EN 55022: 1998

2003-01-06 Thread Jim Conrad

EN 60601-1-2:2001 was just published in the OJ. The CENELEC web site
has not been updated yet.

Best Regards,

Jim

Jim Conrad, Convenor IEC SC62A/MT23
P.O. Box 25
Hamilton, MA 01936 U.S.A.

E-mail:   jc...@shore.net

Phone:  978-468-3909
FAX:  978-468-1034


From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of ITL-EMC User
Group
Sent: Monday, January 06, 2003 12:57 AM
To: Emc-Pstc Group (E-mail)
Subject: EN 60601-1-2/ EN 55022: 1998


Thanks to all who replied.
I was pretty sure about EN 55022: 1998 but wanted to make sure.
Anything about the new edition of IEC/EN 60601-1-2?
 David Shidlowsky
 Technical Writer
 EMC Laboratory
 ITL (Product Testing) Ltd.
 Kfar Bin Nun
 Israel
 Tel: +972-8-9797799
 Fax: +972-8-9797702
 Email: dav...@itl.co.il
 http://www.itl.co.il
 http://www.i-spec.com
 This e-mail message may contain privileged or confidential
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  -Original Message-
 From: ITL-EMC User Group
 Sent: Sunday, January 05, 2003 7:50 AM
 To:   Emc-Pstc Group (E-mail)
 Subject:  EN 60601-1-2/ EN 55022: 1998

 Dear All,
 I have read in various places that the new edition of IEC/EN
60601-1-2 is
 in effect (FDA in the US).
 As yet, only EN 60601-1-2: 1993 is listed in the OJ (December
2002).
 Does anyone know when the new edition will be listed in the OJ and
thus
 become official?
 Regarding EN 55022: 1998 + Amendment A1: 2000, I have also read
that the
 application of this standard is being delayed. Does anyone have
any
 information as to when it will become applicable?
 Thanks
 David Shidlowsky
 Technical Writer
 EMC Laboratory
 ITL (Product Testing) Ltd.
 Kfar Bin Nun
 Israel
 Tel: +972-8-9797799
 Fax: +972-8-9797702
 Email: dav...@itl.co.il
 http://www.itl.co.il
 http://www.i-spec.com
 This e-mail message may contain privileged or confidential
information. If
 you are not the intended recipient, you may not disclose, use,
 disseminate, distribute, copy or rely upon this message or
attachment in
 any way. If you received this e-mail message in error, please
return by
 forwarding the message and its attachments to the sender.




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RE: W32.Elkern removal tools

2002-11-14 Thread Jim Conrad
Do you know if this bug came through the IEEE fire wall?  Any more info
available?  I went to the F-sure site but was unsure if I should download
the removal tool.  Anyone use it yet?

Jim



Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of lfresearch
Sent: Thursday, November 14, 2002 6:12 AM
To: emc-p...@majordomo.ieee.org
Subject: W32.Elkern removal tools

W32.Elkern is a very dangerous virus that can infect on Win98/Me/2000/XP.
F-Secure give you the very W32.Elkern removal tools

For more information,please visit http://www.F-Secure.com


RE: W32.Elkern removal tools

2002-11-14 Thread Jim Conrad
Do you know if this bug came through the IEEE fire wall?  Any more info
available?  I went to the F-sure site but was unsure if I should download
the removal tool.  Anyone use it yet?

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of lfresearch
Sent: Thursday, November 14, 2002 6:12 AM
To: emc-p...@majordomo.ieee.org
Subject: W32.Elkern removal tools

W32.Elkern is a very dangerous virus that can infect on Win98/Me/2000/XP.
F-Secure give you the very W32.Elkern removal tools

For more information,please visit http://www.F-Secure.com


RE: Medical Devices Environmental Requirements

2002-11-05 Thread Jim Conrad

Have you checked 60601-1?

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Naftali Shani
Sent: Tuesday, November 05, 2002 1:27 PM
To: 'Mandel, Joel'; 'emc-p...@majordomo.ieee.org'
Subject: RE: Medical Devices Environmental Requirements


Are there any customers-specific requirements? In the telecom
industry,
NEBS/ETSI (Telcordia GR-63  ETS 300 019) come to mind.

Regards,
Naftali Shani, Catena Networks (www.catena.com)
307 Legget Drive, Ottawa, Ontario, Canada K2K 3C8
613.599.6430/866.2CATENA (X.8277); C 295.7042; F 599.0445
E-mail: nsh...@catena.com

 -Original Message-
From:   Mandel, Joel [mailto:joel_man...@adc.com]
Sent:   Tuesday, November 05, 2002 11:43 AM
To: 'emc-p...@majordomo.ieee.org'
Subject:Medical Devices Environmental Requirements


Hi All
 Can anybody help me out with Environmental testing
requirement/Standards
(Temp,Vibration) for medical devices?
Thank You
Joel Mandel
Reliability Dept
ADC Israel

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RE: RFI/EMI requirements for the automotive industry

2002-10-29 Thread Jim Conrad

Hi Paul,

Take a look at ISO 7637-1 for 12V systems and -2 for 24V vehicles.

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Denomme, Paul
S.
Sent: Tuesday, October 29, 2002 9:16 AM
To: 'emc-p...@majordomo.ieee.org'
Subject: RFI/EMI requirements for the automotive industry


Hi All,

Can someone please inform me of the standards RFI/EMI
standards that
are required in the automitive industry.  This would be for a
microprocessor
controlled item that is part of the vehicle.  My customer stated
that
EMI/RFI specifications are Standard Automotive.  What I am trying
to
figure out is what is Standard Automotive EMI/RFI requirements.

Thank you for your help.

Paul Denomme
Viasystems



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RE: RTCA document vs. IEC 60601-1-02

2002-10-29 Thread Jim Conrad

Thanks Ken,

Yes, 25 dBuV/m not 25 uV/m.  I also found the test set up rather
strange.  Certainly not consistent with CISPR but then the aircraft
environment is entirely different than most other equipment
installations.  I agree, this makes it hard to compare to CISPR
testing.  We may have over simplified the requirements for aircraft
installations.  I will take another look at this.  Any other
information would be very helpful to the IEC working group.  Thanks.


Jim

-Original Message-
From: Ken Javor [mailto:ken.ja...@emccompliance.com]
Sent: Tuesday, October 29, 2002 9:16 AM
To: Jim Conrad; m.bushn...@ieee.org; emc-p...@majordomo.ieee.org
Cc: Jim Conrad
Subject: Re: RTCA document vs. IEC 60601-1-02

I think you mean 25 dBuV/m, but regardless of the number, it is not
a direct
comparison to CISPR because

a) the DO-160 EUT-antenna separation is 1 meter, not 3 or 10 meters,
and

b) the test is performed without an antenna height search, and

c) the EUT is fastened to a metallic ground plane, and EUT-attached
cables
are mounted directly above the ground plane, which reduces emissions
relative to a CISPR test set up.

--
From: Jim Conrad jc...@shore.net
To: m.bushn...@ieee.org, emc-p...@majordomo.ieee.org
Cc: Jim Conrad jc...@shore.net
Subject: RE: RTCA document vs. IEC 60601-1-02
Date: Tue, Oct 29, 2002, 6:48 AM



 I'm not sure if DO-199 or 233 has EMC requirements but I am very
 interested if you come with any.  IEC 62A/MT 23 is in the process
of
 amending 60601-1-2 for medical equipment  used in the aircraft
 environment.  We have based our requirements on the environment
 specified in DO-160.  In general, the DO-160 requirement for RE
are
 higher than CISPR except in the communications and navigation
 frequency bands.  For example, RE dips to 25 uV/m in the 100 - 150
 MHz band for category II equipment.  Please let me know if you
find
 anything in DO-233 that might alter our assumptions.  Thanks.

 Jim

 -Original Message-
 From: owner-emc-p...@majordomo.ieee.org
 [mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of
 m.bushn...@ieee.org
 Sent: Monday, October 28, 2002 4:28 PM
 To: emc-p...@majordomo.ieee.org
 Subject: RE: RTCA document vs. IEC 60601-1-02


 Late reply:
 I have not looked at DO-199, but I noticed that RTCA also has the
 following
 document:
 DO-233 Issued: 08/20/1996
 Description: This document addresses the potential interference to
 installed
 aircraft electrical and electronic systems from Portable
Electronic
 Devices
 (PEDs) carried aboard by passengers. It defines the potential
 interference
 phenomena; outlines the risk potential from interference events;
 provides test
 methods to determine whether or not a potential for interference
 exists for
 certain PEDs, aircraft and combinations thereof; and addresses
 acceptable
 levels of interference. The report also recommends modification of
 Federal
 Aviation Regulation 91.21, continued PEDs testing to identify and
 better define
 the possibility of interference to aircraft electronic systems,
 increased
 public awareness of the potential for interference from PEDs, and
 the
 development and use of devices to detect spurious PEDs emissions.

 FYI, here is the descriptions for DO-199 Volumes I and II:
 DO-199 Issued: 09/16/1988
 Description: Reports on the investigation to determine potential
 interference
 effects to aircraft electronic systems due to emissions from
 self-powered
 portable electronic and electrical devices operated aboard
aircraft.
 Recommends
 regulatory actions relating to operation and identification of
 passenger-
 operated devices to assure control of possible sources of
 interference, and
 recommends standardized procedures for reporting suspected
 interference. Volume
 I is the basic report and includes background, data collection,
data
 analysis,
 conclusions and recommendations. Volume II provides amplification
or
 background
 material for some of the summary data included in the basic
report.
 Superseded
 DO-119

 Sincerely,
 Mark E. Bushnell, Technical Writer IEEE EMC P299 WG
 m.bushn...@ieee.org
 L-3 communications Integrated Systems, Greenville, Texas
 Tel. 903.457.6375  Fax 903.457.4413
 This message is printed on 100% recycled electrons.
 
 --
 From:   Ron[SMTP:r...@vascor.com]
 Reply To:   Ron
 Sent:   Friday, September 13, 2002 01:58 PM
 To: EMC
 Subject:RTCA document vs. IEC 60601-1-02


 I recently came across a synopsis of document DO-199, Potential
 Interference to Aircraft Electronic Equipment from Devices Carried
 Aboard.
 Since I don't have the complete document, does anyone know if this
 document
 contains EMC specs/limits on RF emissions, etc.  Are these the
same
 specs/limits as outlined in IEC 60601-1-02?  ... same as CISPR 11?

 ---
 This message is from the IEEE EMC Society Product Safety
 Technical Committee emc-pstc discussion list.

 Visit our

RE: RTCA document vs. IEC 60601-1-02

2002-10-29 Thread Jim Conrad

I'm not sure if DO-199 or 233 has EMC requirements but I am very
interested if you come with any.  IEC 62A/MT 23 is in the process of
amending 60601-1-2 for medical equipment  used in the aircraft
environment.  We have based our requirements on the environment
specified in DO-160.  In general, the DO-160 requirement for RE are
higher than CISPR except in the communications and navigation
frequency bands.  For example, RE dips to 25 uV/m in the 100 - 150
MHz band for category II equipment.  Please let me know if you find
anything in DO-233 that might alter our assumptions.  Thanks.

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of
m.bushn...@ieee.org
Sent: Monday, October 28, 2002 4:28 PM
To: emc-p...@majordomo.ieee.org
Subject: RE: RTCA document vs. IEC 60601-1-02


Late reply:
I have not looked at DO-199, but I noticed that RTCA also has the
following
document:
DO-233 Issued: 08/20/1996
Description: This document addresses the potential interference to
installed
aircraft electrical and electronic systems from Portable Electronic
Devices
(PEDs) carried aboard by passengers. It defines the potential
interference
phenomena; outlines the risk potential from interference events;
provides test
methods to determine whether or not a potential for interference
exists for
certain PEDs, aircraft and combinations thereof; and addresses
acceptable
levels of interference. The report also recommends modification of
Federal
Aviation Regulation 91.21, continued PEDs testing to identify and
better define
the possibility of interference to aircraft electronic systems,
increased
public awareness of the potential for interference from PEDs, and
the
development and use of devices to detect spurious PEDs emissions.

FYI, here is the descriptions for DO-199 Volumes I and II:
DO-199 Issued: 09/16/1988
Description: Reports on the investigation to determine potential
interference
effects to aircraft electronic systems due to emissions from
self-powered
portable electronic and electrical devices operated aboard aircraft.
Recommends
regulatory actions relating to operation and identification of
passenger-
operated devices to assure control of possible sources of
interference, and
recommends standardized procedures for reporting suspected
interference. Volume
I is the basic report and includes background, data collection, data
analysis,
conclusions and recommendations. Volume II provides amplification or
background
material for some of the summary data included in the basic report.
Superseded
DO-119

Sincerely,
Mark E. Bushnell, Technical Writer IEEE EMC P299 WG
m.bushn...@ieee.org
L-3 communications Integrated Systems, Greenville, Texas
Tel. 903.457.6375  Fax 903.457.4413
This message is printed on 100% recycled electrons.

--
From:   Ron[SMTP:r...@vascor.com]
Reply To:   Ron
Sent:   Friday, September 13, 2002 01:58 PM
To: EMC
Subject:RTCA document vs. IEC 60601-1-02


I recently came across a synopsis of document DO-199, Potential
Interference to Aircraft Electronic Equipment from Devices Carried
Aboard.
Since I don't have the complete document, does anyone know if this
document
contains EMC specs/limits on RF emissions, etc.  Are these the same
specs/limits as outlined in IEC 60601-1-02?  ... same as CISPR 11?

---
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RE: RADIATED IMMUNITY TESTING ABOVE 1GHz

2002-10-01 Thread Jim Conrad

John Woodgate wrote:

There was a BIG argument between experts over the test signal to be
used
for assessing immunity to mobile phone emissions. CENELEC people
prematurely chose the keyed-carrier signal, but it presents
inconvenience in both generation and measurement. IEC experts (some
from
Europe) showed that sinusoidal modulation is quite acceptable and
does
not present those problems. See Annex A of IEC/EN61000-4-3:1995/7.
--
I agree with John's comments.  I have also done the comparison
between on-off keying and sine wave modulation and found almost no
difference on medical products.  They measured to have the same
susceptibility with either modulation.  We conducted the test up to
@.5 GHz.   It was a joint effort between Motorola and HP/Agilent.  I
hope this helps.

Best regards,

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of John Woodgate
Sent: Monday, September 30, 2002 9:20 AM
To: emc-p...@majordomo.ieee.org
Subject: Re: RADIATED IMMUNITY TESTING ABOVE 1GHz


I read in !emc-pstc that Gordon,Ian ian.gor...@edwards.boc.com
wrote
(in E1BA0362B28ED211A1E80008C71EA306018190CE@EXC_EAS01) about
'RADIATED IMMUNITY TESTING ABOVE 1GHz' on Mon, 30 Sep 2002:
My mistake - the old light industrial generic immunity standard
EN50082-1
(and EN61000-6-1?) includes use of a keyed carrier at 900MHz

No, IEC/EN 61000-6-1 doesn't include it either.

There was a BIG argument between experts over the test signal to be
used
for assessing immunity to mobile phone emissions. CENELEC people
prematurely chose the keyed-carrier signal, but it presents
inconvenience in both generation and measurement. IEC experts (some
from
Europe) showed that sinusoidal modulation is quite acceptable and
does
not present those problems. See Annex A of IEC/EN61000-4-3:1995/7.
--
Regards, John Woodgate, OOO - Own Opinions Only.
http://www.jmwa.demon.co.uk
Interested in professional sound reinforcement and distribution?
Then go to
http://www.isce.org.uk
PLEASE do NOT copy news posts to me by E-MAIL!

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RE: EN 60601-1-2

2002-09-24 Thread Jim Conrad

It seems a bit strange that they have not listed it in the OJ yet
but I am told it is coming soon.  I think the important thing is
that CENELEC approved it in Sept of 2001 and have now published the
DOR, DOP, DOW on their web site.  Now we just have to wait for the
OJ publication that should happen in November.

Best Regards,

Jim

Jim Conrad, Convenor IEC SC62A/MT23
P.O. Box 25
Hamilton, MA 01936 U.S.A.

E-mail:   jc...@shore.net

Phone:  978-468-3909
FAX:  978-468-1034

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of ITL-EMC User
Group
Sent: Tuesday, September 24, 2002 2:51 AM
To: emc-p...@majordomo.ieee.org
Subject: EN 60601-1-2


Hi all,
Has anyone heard when the latest edition of EN 60601-1-2 will be
published
in the Official Journal?
I have received enquiries from customers regarding the new edition.
Thanks to anyone who can help.
Regards

David Shidlowsky
Technical Writer
EMC Laboratory
ITL (Product Testing) Ltd.
Kfar Bin Nun
Israel
Tel: +972-8-9797799
Fax: +972-8-9797702
Email: dav...@itl.co.il
http://www.itl.co.il
http://www.i-spec.com
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RE: Medical Wrist Device and Cardiac Pacemakers

2002-09-18 Thread Jim Conrad

Hi Peter,

I'm not sure what your wrist device does.  Does it have electronics
in it with clock frequencies over 9 kHz?  Does it transmit a EMF?
If the device is within CISPR limits then you should be OK for
pacemakers.  I think they are tested at 100 V/m.  Some pacemakers
have a magnetic switch in them that is activated at 10 gauss.   I
will send you a document describing EMI for pacemakers separately.

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Peter
Merguerian
Sent: Tuesday, September 17, 2002 8:21 AM
To: EMC-PSTC (E-mail) 
Subject: Medical Wrist Device and Cardiac Pacemakers


Dear All,

For a medical device to be worn on the wrist of a patient, does
anyone know
what additional requirements (if any) should the manufacturer of the
medical
device take in order for the device not to interfere with a cardiac
pacemaker?

My little research on the subject tells me that the cardiac
pacemaker
manufacturer should take all the required measures so that any other
device
nearby (cellular telephones, medical equipment, etc.) does not
interfere
with the pacemaker. Is this correct?


Best Regards

This e-mail message may contain privileged or confidential
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PETER S. MERGUERIAN
Technical Director
I.T.L. (Product Testing) Ltd.
26 Hacharoshet St., POB 211
Or Yehuda 60251, Israel
Tel: + 972-(0)3-5339022  Fax: + 972-(0)3-5339019
Mobile: + 972-(0)54-838175
http://www.itl.co.il
http://www.i-spec.com





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RE: SMPS EMC Emissions

2002-09-03 Thread Jim Conrad

Alex wrote:

Do you think it is reasonable to specify in my power supply
specification
that the manufacturers SMPS should meet EN55022 Class B -6dB

Yes.  I would ask for 6 dB margin since measurement uncertainty for
a typical conducted measurements system is 5.4 dB.   You must also
allow for unit to unit variations in manufacturing.  Sample 5 units
and apply the 80/80 rule and see if they still pass.

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Alex McNeil
Sent: Tuesday, September 03, 2002 4:57 AM
To: 'emc-p...@majordomo.ieee.org'
Subject: SMPS EMC Emissions


Hi Group,

First of all thank you to those who replied to my previous email. I
have not
had time to reply personally...yet.

I have noticed that the broadband noise of some SMPS are already
near to the
limits of EN55022 Class B (I tested with a max resistive load). This
gives
my product little scope for emissions at these broadband
frequencies,
especialy when my product is taking peak load e.g. printing.

The power supply manufacturer rightly claims that his product does
meet
EN55022 Class B.

Do you think it is reasonable to specify in my power supply
specification
that the manufacturers SMPS should meet EN55022 Class B -6dB or?
Have any of you come across a similar scenario?

As usual , I look forward to your professional opinions.

Kind Regards
Alex McNeil
Principal Engineer
Tel: +44 (0)131 479 8375
Fax: +44 (0)131 479 8321
email: alex.mcn...@ingenicofortronic.com


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RE: Transmission line formula?

2002-08-29 Thread Jim Conrad

Hi Brent,

I had the same problem when I designed mine.  By using square stock,
which is great for building a log-p, I was  not able to get the
impedance necessary to make it look 50 ohms at the driving end(but
close enough to keep the VSWR  2:1).  I was also trying to push the
limits on gain and size.  In any event, I finally wound up measuring
the characteristic Z of the square stock transmission line.  At
close spacing the formula is Zo=377(w/l) for l/w10.  w is the
spacing and l is the thickness of the rod.  If l/w is 0.1 then use
Zo=120*cosh-1(w/l)  or Zo=276*log(2w/l).  If you are in the area of
w=l then use Zo=sqrt(L/C) where L is the inductance per unit length
and C is the capacitance per unit length.  Measure these on your HP
impedance or network analyzer.  This gets you very close.  Good
luck!  Give me a call if you would like more info.

Best Regards,

Jim

Jim Conrad
Conrad EMC Consulting
P.O. Box 25
Hamilton, MA 01936 U.S.A.

E-mail:   jc...@shore.net

Phone:  978-468-3909
FAX:  978-468-1034

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of
brent.dew...@us.datex-ohmeda.com
Sent: Wednesday, August 28, 2002 6:26 PM
To: emc-p...@majordomo.ieee.org
Subject: Transmission line formula?


Anyone have a formula for calculating the Z0 of two parallel
rectangular
pieces of metal tubing in air?  I'm designing a log-periodic antenna
and
need to get the boom transmission line spacing right.

Thanks!

Brent DeWitt
Datex-Ohmeda


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RE: Bonding to conductive plastic - best method??

2002-06-02 Thread Jim Conrad
Hi Chris,

I would try a Silver loaded conductive epoxy or use SS self tapping screws.

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Chris Wells
Sent: Friday, May 31, 2002 10:23 PM
To: EMC-PSTC Discussion Group
Subject: Bonding to conductive plastic - best method??


- Original Message -
From: Chris Wells mailto:cdwe...@adelphia.net
To: EMC-PSTC Discussion Group mailto:emc-p...@majordomo.ieee.org
Cc: christopherdwe...@eaton.com mailto:christopherdwe...@eaton.com
Sent: Friday, May 31, 2002 8:07 AM
Subject: Bonding to conductive plastic - best method??

Recently we had a good string going on conductive platics.
I would appreciate some help coming up with the ideal electrical bond to
this type of plastic.

We use a 6% Stainless Steel Fiber mix in Poly carbonate and I was looking
for the best method to electrically bond to the plastic to drain off ESD or
for high frequency bonding with the metal portion of our product.  This
would include Printed Circuit Board to plastic, Cable to plastic and metal
housing to plastic type connections.
For joining metal housing and PCB connections we have been using plastic
screws that mechanically are designed for plastic.
The threads are widely spaced, tall and thin - They cut into the plastic
with out breaking the mounting bosses (studs).
The engagement with the plastic (screw thread in plastic boss hole) is ~
100% leaving little or no air gap between the screw and the plastic.

First set of Question -
If using screws what would be the best type of screw to insure good contact
to the stainless steel fibers?
* High profile, thin thread, plastic screw like I described?
* Self tapping type screw?

What should the platting be?
* Clear Zinc
* Zinc Chromate?
* Nickle on brass?
* Stainless Steel?

Is there any sort of liquid/paste like adative that could be added to the
screw hole to enhance the electrical connection?

We have experimented with metal inserts (PEM nut brand for example).
What sort of bonding does one get when molded in?  I suspect poor relative
to press in.
Can the inserts be plain brass or should they be plated like with nickle?
Depth of inserts - Longer inserts should be better but I am concerned about
cracking of the boss.

Screen matterial in the screw boss.
I have seen screen matterial embedded in conductive plastic.
Perhaps it could help screws bond to the plastic as well.
Any comments?  Sounds messy.

Coatings on top of conductive plastic?
If a coating were placed on the inner surface of the conductive plastic it
might make a good hybrid sollution but costly.

Are there other considerations?
If you respond today try CC to
christopherdwe...@eaton.com mailto:christopherdwe...@eaton.com
So I get it at work too (the ITE guys can't handle this subscription list at
work)
This group is the best resource I have for this sort of topic - thanks in
advance!!

Chris Wells
Senior Design Engineer
Cutler-Hammer
Pittsburgh, Pa. USA
christopherdwe...@eaton.com mailto:christopherdwe...@eaton.com





RE: non 601 approved isolating component

2002-05-02 Thread Jim Conrad

Hi Ron,

I think I am using the same part.  Is it the isoloop part?
That part is good for 2.5 kV for one minute.  We plan to do
humidity soak and dielectric tests to show that the basic
insulation of the part is adequate for 601-1.  I have also
talked to the vendor to get the part UL2601 listed.  There
are several other medical customers using the part.  The
device is built to the same requirements/specs as the opto
isolators so I have good feeling it is OK for our
application (60601-1).  Just be aware that some of the parts
don't quite meet the 30 kV/uS transient immunity spec. and
they do not spec the magnetic immunity.  As you know, 3 A/m
is required by 601.  They jitter like crazy when you bring a
50/60 Hz field next to them.  What freq. will you be running
them at?  They have higher immunity at 5 Volts supply
voltages.


Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Ron
Sent: Wednesday, May 01, 2002 2:49 PM
To: EMC
Subject: non 601 approved isolating component


I need to use an isolating device between a sip/sop and an
applied part (BF)
requiring 1500V isolation (Basic(250)).  I plan on using a
digital isolator,
but the component does not have IEC601 approval.  The
component does have
2500V isolation and 8 mm creepage.

Questions:

1) When our product is submitted for IEC601 certification,
how does the use
of the non 601 approved part affect the investigation?

 2) Does the investigator need the schematic for that
component?  What if
the schematic is not available?

 3) If the component already has other approvals (UL1950 or
UL1577).  How
does this affect the approval process?

Thanks in advance.

r...@vascor.com


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RE: Work in progress vs Date of Withdrawal

2002-03-22 Thread Jim Conrad

Hi Al,

I do not know of a guide but it is usually stated in the directive what
placing a product on the market means.  It is my understanding that you
can not ship(place on the market) anything into the EC that carries the CE
mark after the date of withdrawal of a standard that is used to show
compliance to a directive.  Any products that are stored in a warehouse in
the EC can still be sold after the DOW.  Work in progress does not count.
It must be in the country.

Best regards,

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Brewster, Alan
Sent: Friday, March 22, 2002 10:52 AM
To: emc-pstc
Subject: Work in progress vs Date of Withdrawal


Greetings All,
If a vendor is in the process of building equipment and has started the
manufacturing phase before the date on which a standard is superceded, can
the goods still be supplied against the old standard? In particular, the
introduction of EN 61000-6-2 on April 1st will leave some equipment
suppliers with long lead time parts in a quandary over how to declare,
especially if they might not meet the surge and dip requirements.
Is there a published guidance on the treatment of material that is Work in
Progress?

Regards,

Alan Brewster



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RE: SDR in the US

2002-03-16 Thread Jim Conrad

Hi Kim,

902-928 MHz is an Amateur Radio band in the US and I don't think it is
available for general use.  I am sending you an FCC publication entitled
UNDERSTANDING THE FCC REGULATIONS FOR LOW-POWER, NON-LICENSED
TRANSMITTERS.   I hope it helps.

Best regards,

Jim



-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Kim Boll Jensen
Sent: Friday, March 15, 2002 7:36 AM
To: treg; EMC-PSTC
Subject: SDR in the US

Hi all

I have a Radio remote control for use in private homes

I have understood that 433MHz SRD is not possible in the US in the same
way as in EU.

Some FCC notes points to 902 - 928 MHz for this kind of equipment.

I'm trying to understand the FCC but I'm hindered by no possible
download of relevant 47CFR code

(http://www.access.gpo.gov/nara/cfr/waisidx_00/47cfr90_00.html doesn't
seem to function at the moment)

Is it correct that 902 -928 is allowed in part 15 without license if
output is below 50mV/m at 3m, and if I need more power I will have to
apply for a general license under part 90 ?

Please help me !


Best regards,

Kim Boll Jensen
Bolls Raadgivning
Denmark


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RE: Industrial Locations

2002-02-20 Thread Jim Conrad

Amund,

I am curious why you included ISM in your list of industrial locations.  ISM
can be either class A  or class B.  I thought the distinction was made
according to the mains power distribution system; CISPR 11, subclause 4.2.

JIm

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of
am...@westin-emission.no
Sent: Tuesday, February 19, 2002 2:23 PM
To: emc-p...@majordomo.ieee.org
Subject: SV: Industrial Locations


I only have the generic EN50082-2 (immunity) and EN50081-2 (emission)
standards, so I quote the description of locations from these standards:
QUOTE start
Industrial locations are characterized by the existence of one or more of
the following conditions:
- industrial, scientific and medical apparatus are present
- heavy inductive or capacitive loads are frequently switched
- current and associated field are high
These are the major contributors to the industrial electromagnetic
environment and as such distinguish the industrial from other environments.
QUOTE end

There are no other industrial examples in these generic standards.

Amund, Oslo/Norway


-Opprinnelig melding-
Fra: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]På vegne av
richwo...@tycoint.com
Sendt: 19. februar 2002 15:45
Til: emc-p...@majordomo.ieee.org
Emne: Industrial Locations



Do the Generic emission and immunity ENs for industrial locations provide
examples of those locations? If so, I would appreciate someone providing the
list of the example locations. I need to compare them against the examples
of light-industrial locations. Thanks in advance.


Richard Woods
Sensormatic Electronics
Tyco International


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RE: Medical Device Emissions Limit?

2002-02-12 Thread Jim Conrad

Yes it is.  The real frequency is 450 kHz ±100 kHz.

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of John Woodgate
Sent: Tuesday, February 12, 2002 8:04 AM
To: emc-p...@majordomo.ieee.org
Subject: Re: Medical Device Emissions Limit?


I read in !emc-pstc that Jim Conrad jc...@shore.net wrote (in
ncbbkfbmfdcdcgaccfbaaeimgmaa.jc...@shore.net) about 'Medical Device
Emissions Limit?', on Tue, 12 Feb 2002:

ESU = Electro Surgical Unit -  also know as the Bovie knife

As opposed to Bowie. Or the German version thereof.

and is used for
cutting and coagulating in the operating room.  It is essentially a 300
watt
spark gap transmitter operating at 500 kHz.

Charming! Isn't that still an International Distress Frequency?
--
Regards, John Woodgate, OOO - Own Opinions Only. http://www.jmwa.demon.co.uk
After swimming across the Hellespont, I felt like a Hero.
PLEASE do NOT copy news posts to me by E-MAIL!

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RE: Medical Device Emissions Limit?

2002-02-12 Thread Jim Conrad

ESU = Electro Surgical Unit -  also know as the Bovie knife and is used for
cutting and coagulating in the operating room.  It is essentially a 300 watt
spark gap transmitter operating at 500 kHz.

Sorry about that.

Best regards,

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of John Woodgate
Sent: Monday, February 11, 2002 10:47 PM
To: emc-p...@majordomo.ieee.org
Subject: Re: Medical Device Emissions Limit?


I read in !emc-pstc that Jim Conrad jc...@shore.net wrote (in
ncbbkfbmfdcdcgaccfbageihgmaa.jc...@shore.net) about 'Medical Device
Emissions Limit?', on Mon, 11 Feb 2002:
you should also consider ESU testing even thought it is not
specifically mentioned (at this time) in standards you mentioned below.

What is 'ESU testing'?
--
Regards, John Woodgate, OOO - Own Opinions Only. http://www.jmwa.demon.co.uk
After swimming across the Hellespont, I felt like a Hero.
PLEASE do NOT copy news posts to me by E-MAIL!

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RE: Medical Device Emissions Limit?

2002-02-12 Thread Jim Conrad

Hi Kevin,

Hospitals are generally considered Class A.  If the device will be used in
the OR, you should also consider ESU testing even thought it is not
specifically mentioned (at this time) in standards you mentioned below.
Your customers in the OR will be real unhappy when the Bovie goes off and
your product fails to function.

Best regards,

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Kevin Hight
Sent: Monday, February 11, 2002 11:16 AM
To: emc-p...@majordomo.ieee.org
Subject: Medical Device Emissions Limit?


Good Morning,

I am in desperate need of your expert assistance.  I need to define the
requirements for a device that is located in a hospital operating room.

Device 'X' is used during surgery and makes contact to the patient.

The device will be compliant with EN 60601-1, EN 60601-1-1,  EN 60601-1-2
(2001).

Question:
For Radiated Emissions, is this product a Class A or a Class B device?



Regards,

__
Kevin J. Hight - Principal Compliance Engineer
Colorado MEDtech, Inc.
6175 Longbow Drive, Boulder, Colorado 80301
Phone: (303) 530-8288 x-3111   Fax: (303) 581-1003
Email: k...@cmed.com mailto:k...@cmed.comhttp://www.cmed.com
http://www.cmed.com
Great crises produce great men, and great deeds of courage. -- John F.
Kennedy


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RE: IEC 60601-1-2 Second Edition

2002-02-05 Thread Jim Conrad

Hi Ned,

I think everyone is asking the same question.  You have received the correct
interpretation from the FDA.  The 2nd edition is effective as of 10-2001 and
if you claim compliance with it on your 510k, the FDA will not come back and
ask for more information regarding EMC.  They are however reasonable and do
not expect manufactures to comply on such short notice but they then also
reserve the right to come back and ask you additional questions regarding
the EMC performance of you product which may include why you did not choose
to comply with the 2nd edition of 60601-1-2.  Call me if you want more
information regarding this.

You asked: Has anyone had any success in doing a risk analysis to use lower
immunity
compliance levels than specified in IEC 60601-1-2, Second Edition, Section
36.202.1 a) or using different compliance criteria (36.202.1 j))?   The
risk analysis that is call for in the 2nd edition is only to determine which
functions of the equipment will be tested for immunity.  Only those
functions that are associated with essential performance need be tested.
A risk analysis does not allow essential performance to pass at reduced
levels.

Yes, Clause 6.8.3.201 a) 5), These justification shall be based only on
physical, technological or physiological limitations... pretty much
preclude the use of lower limits?  Your justification for lower immunity
levels must be based on  physical, technological or physiological
limitations.

You stated and asked: The device in question meets IEC 60601-1-2 First
Edition, but will not pass
the requirements in the Second Edition.  Can the justification be that
since there are no known risks on the device, the current level of immunity
is adequate?  No you cannot use this as a justification because it is not
based on physical, technological or physiological limitations of your
equipment.

Please contact me directly if you need more help.

Best regards,

Jim








-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Ned Devine
Sent: Tuesday, February 05, 2002 4:24 PM
To: IEEE EMC/Product Safety (E-mail)
Subject: IEC 60601-1-2 Second Edition


Hi,

I need some help from the EMC experts.

According to FDA Acting Chief of the Brach I am dealing with, since the FDA
has recognized IEC 60601-1-2 Second Edition (October 2001), then ...If they
submit a new 510(k) (or even a modification for an existing device) and we
have recognized the more recent standard, then they would need to comply
with the new standard.   Making the new edition immediately effective seems
a little harsh.  I am appealing his interpretation, but I don't know if I
will have any luck.

Has anyone had any success in doing a risk analysis to use lower immunity
compliance levels than specified in IEC 60601-1-2, Second Edition, Section
36.202.1 a) or using different compliance criteria (36.202.1 j))?  Or does
Clause 6.8.3.201 a) 5), These justification shall be based only on
physical, technological or physiological limitations... pretty much
preclude the use of lower limits?

The device in question meets IEC 60601-1-2 First Edition, but will not pass
the requirements in the Second Edition.  Can the justification be that
since there are no known risks on the device, the current level of immunity
is adequate?

Thanks

Ned

Ned Devine
Program Manager
Entela, Inc.
3033 Madison Ave. SE
Grand Rapids, MI  49548

1 616 248 9671 Phone
1 616 574 9752 Fax
ndev...@entela.com e-mail



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No 

RE: noise immunity on mains powered equipment

2002-01-30 Thread Jim Conrad

Ken, I don't recall your original  query but it sounds like you were asking
about BCI testing requirements.  I can answer for medical equipment.  The
2nd ED of 60601-1-2 requires BCI testing of all patient connected cables.

Best regards,

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Ken Javor
Sent: Thursday, January 24, 2002 11:49 AM
To: kristiaan.carpent...@alcatel.be; 'EMC-PSTC'
Subject: Re: noise immunity on mains powered equipment


I was hoping someone would be able to answer this more authoritatively than
I can, but if there have been any replies, I missed them.  I am aware that
the US FDA imposes a BCI type requirement like MIL-STD-461 CS114.  Of course
that is for medical equipment.  RTCA/DO-160 imposes a very similar BCI
requirement on commercial avionics.  SAE ARP 1972 included BCI testing but
was just a recommended practice, I don't know of any entity that actually
levied it as a requirement.  The automotive world in this country at least
has adopted BCI techniques as well.  There were in-house specs (I recall
seeing a GM spec) and a better version has been adopted as an SAE J-type
requirement industry-wide.  That's about all I can think of off the top of
my head.

--
From: kristiaan.carpent...@alcatel.be
To: 'EMC-PSTC' emc-p...@majordomo.ieee.org
Subject: noise immunity on mains powered equipment
Date: Wed, Jan 23, 2002, 11:06 AM



 Hello,

 Has any-one ever heard about a standard (non-military) that describes
noise
 immunity of mains powered equipment.
 Testing seems to be done by the current bulk injection method. the
standard
 is not IEC 61000-4-6.
 Regards,
 Kris Carpentier


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RE: IEC 60601-1/EN 60601-1 Question

2002-01-23 Thread Jim Conrad

Hi Kaz,

I agree with Jon.  However there are battery standards that you may consider
meeting if you plan on CE marking the battery so it can be imported and sold
in Europe as an accessory to your device.  I just went through this with a
recent medical product I worked on.  There are also requirements for battery
operated MEE in 60601-1-2; 2001 that you may want to consider.  Best of
luck.

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Jon Griver
Sent: Tuesday, January 22, 2002 4:13 PM
To: emc-p...@majordomo.ieee.org
Cc: kazimier_gawrzy...@dell.com
Subject: IEC 60601-1/EN 60601-1 Question


Kaz,

I have checked my copy of EN 60601-1:1990 with amendments A1:1992 A2:1995
and A13:1995, which is the version of the standard currently specified in
the Official Journal.

I can find no reference to any specific battery standards in Annex L or
Annex ZA. Clause 56.7 of the standard does have general requirements for
batteries.

Regards,

Jon Griver
www.601help.com
The Medical Device Developers Guide to IEC 60601-1



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RE: EMC for cardio : which standard apply?

2002-01-09 Thread Jim Conrad

Hi Paolo,

Yes, the 2nd ED has additional requirements but you will need to meet them
anyway by November 2004 which is the D.O.W. for the 1st ED of 60601-1-2.  In
addition, the FDA in the US is now looking for compliance to the 2nd ED.
That is, if you claim compliance to the 2nd ED on your 510K then they can
not ask you for additional information about EMC.  Japan also recognizes the
2nd ED.

With all that being said, you can still use the 1st ED for CE compliance
until November 2004.   After that date, any MEE shipped into Europe with the
CE mark will have to meet the requirements of the 2nd ED if you are going
the standards route of compliance to the MDD.  I hope this helps.

Jim

-Original Message-
From: Paolo Peruzzi [mailto:paolo.peru...@esaote.com]
Sent: Wednesday, January 09, 2002 2:53 AM
To: Jim Conrad
Cc: emc-p...@majordomo.ieee.org
Subject: RE: EMC for cardio : which standard apply?


Jim,
thanks for your suggestions.
Our product will be sold at least in Europe and US, so we need CE marking,
but not only that, I suppose.
Though there are some similarities between 60601-2-25 +A1 and 60601-1-2 2nd
ed, I think there are important differences too, to the extent that the
latter is in general more severe (more tests prescribed).
Best regards,
p.p.

-
ESAOTE S.p.A. Paolo Peruzzi
Research  Product DevelopmentDesign Quality Control
Via di Caciolle,15tel:+39.055.4229306
I- 50127 Florence fax:+39.055.4223305
e-mail: paolo.peru...@esaote.com



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RE: IEC 601-1 : Insulation between applied part and signal input

2001-12-29 Thread Jim Conrad
Hi Pierre,

How is the skiing this year?

Regarding your question, you need to look at the system standard, 60601-1-1,
for interconnecting components of a medical electrical system.  Generally, a
computer does not meet the enclosure leakage requirements and thus requires
some kind of an isolation device between the computer and the medical
device.  This could be an optical coupled RS 232 port as you described.
This maybe the best way to achieve electrical safety.  There are other ways
such as the use of the EQUAL POTENTIAL GROUND wire.   This is a quick answer
but you need to study 60601-1-1 to determine the correct method of
protection and also labeling requirements.  Best of luck and Happy New Year.

Jim



-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Pierre SELVA
Sent: Thursday, December 27, 2001 4:25 PM
To: Forum Safety-emc
Subject: IEC 601-1 : Insulation between applied part and signal input

Hello from the Franch Alps,

I need your help to determinate which insulation is required between an
applied part (lin to the OV of the product thru a capacitor) and one signal
input in a medical product, against IEC 601-1 requirements.
The signal input is connected to the parallel port of a computer.
I understand that the insulation has to be a supplementary one.
Does this mean that I need to have a galvanic insulation (with optocoupleur,
for example) or can I use another system ?

Thanks a lot for your contribution.

Bonnes fêtes de fin d'année et meilleurs voeux pour 2002 (happy new year and
best whishes !)

eLABs
Pierre SELVA
18 Rue Marceau Leyssieux
38400 SAINT MARTIN D'HERES - FRANCE
Phone : 33 (0)6 76 63 02 58
Fax : 33 (0)6 61 37 87 48
e-mail : e.l...@wanadoo.fr mailto:e.l...@wanadoo.fr
ps.el...@laposte.net mailto:ps.el...@laposte.net
==



RE: Field Strength - Substitution Method

2001-12-27 Thread Jim Conrad

Sam,

You should also consider the radiation may be from multiple sources on the
EUT.  Polarization of the source may not be the same at the substitution
antenna.  Try 0, 45, and 90 degree polarization of the bi-con.  A tuned
dipole would also give you better results as a bi-con has a very high SWR.
This gives you addition loose which you may not have accounted for.

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Cortland Richmond
Sent: Thursday, December 27, 2001 12:26 PM
To: Sam Wismer; ieee pstc list
Subject: Re: Field Strength - Substitution Method


Sam,

I think you did it right with one AF and one gain. There's a problem with
that method.  You need more information needed to make the  _results_
right.

Given a certain power at the antenna terminal, and a known gain and
efficiency, you can calculate the free-space field strength at some
distance due to RF applied to that antenna. Then you add loss or gain due
to reflection from the ground plane.

This gets you down to some fairly reliable way to estimate what field
strength will be created over a ground plane at some distance from an
antenna.

What you don't have -- and what, I think, is most difficult -- is a model
that reliably correlates a substitution antenna as a source with the
equipment under test. A rack seven feet tall and two feet on a side -- with
wires overhead and off to its sides -- will NOT radiate the same as a
dipole. And it will differ more from an antenna as its dimensions become
larger than the antenna. I would expect differences to become more
pronounced, in other words, at higher frequencies. This is what you saw.

Cortland
(my own opinion and not that of my employers)

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RE: -2dB margin

2001-12-27 Thread Jim Conrad

Hi George,

I don't think the margin makes any difference in applying the 80/80 rule.
If you have a series produced product you must apply the 80/80 rule using a
sample size of not less than 5 and not more than 12 pieces.  See Clause 11,
Assessment of conformity of equipment, of CISPR 11: 1999.

Happy New Year to all!

Best regards,

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of George Stults
Sent: Monday, December 24, 2001 2:43 PM
To: 'emc-p...@majordomo.ieee.org'
Subject: -2dB margin


Hello Group,

I've been looking into the 80/80 rule for CISPR 22 compliance for mass
produced equipment.   I have found a description of the statistics in  CISPR
22 :1997  Section 7.1 and 7.2.  Its been my understanding that for testing
at OATS,  if the product has 2dB or less margin, then these statistical
methods are required.  Is that correct?  And, where does the reference to
'2dB margin' come from?

Thanks in  advance

George S.


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RE: Enclosed OATS facilities in snow country

2001-12-13 Thread Jim Conrad
We plow the snow away from around the building.  Unfortunately the building
is up on a small rise but it does make it easy to get the snow line below
the ground plane.

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Bill Owsley
Sent: Wednesday, December 12, 2001 2:10 PM
To: geor...@lexmark.com; Patrick Lawler
Cc: EMC-PSTC
Subject: Re: Enclosed OATS facilities in snow country

The IBM Greenock lab had an OATS with a very steep roof line, sharp A frame,
and the heat to keep folks warm inside kept the lower edges somewhat free of
snow.  I don't recall any concerns, because the snow was not on top.

- Bill


At 01:06 PM 12/12/2001 , geor...@lexmark.com wrote:





Once upon a time, before we were spun off from IBM, and I was the
EMC manager here, I faintly recall that the IBM Boebligen lab in
Germany had an OATS facility.  I also faintly recall that snow on
the rooftop did impact the measurements needed.

Note that OATS structures are normally constructed with non-conductive
materials, e.g. wood, plastic, etc.  A layer of snow represents a plane
of conductive material, albeit not a great conductor.

However, these are memories from the distant past. Surely there are
some still using OATS facilities where winter snow is a problem.

George




plawler%west@interlock.lexmark.com (Patrick Lawler) on 12/12/2001
12:40:35
PM

Please respond to plawler%west@interlock.lexmark.com (Patrick Lawler)

To:   EMC-PSTC emc-pstc%ieee@interlock.lexmark.com
cc:(bcc: George Alspaugh/Lex/Lexmark)
Subject:  Enclosed OATS facilities in snow country




I saw some photographs of an enclosed OATS facility in an area subject to
snow.

How does snow accumulation on the roof affect performance measurements?
Does it
affect the NSA figures?
Is the effect significant enough that attempts are made to keep the roof
snow
free?  Or does the normal attempt at keeping the inside test area warm
enough
for people take care of snow build-up?





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Bill Owsley,   ows...@cisco.com
919) 392-8341

Compliance Engineer
Cisco Systems
7025 Kit Creek Road
POB 14987
RTP. NC. 27709
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RE: EMI guard bands

2001-12-10 Thread Jim Conrad

Cecil,

We design our products for -10 dB limit,  accept -8 dB for a lab prototype
 pre-production) and allow -6 dB for production units.  We feel this is not
conservative based on past history of measurement uncertainty and production
variations.

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of
cecil.gitt...@kodak.com
Sent: Monday, December 10, 2001 7:46 AM
To: emc-p...@majordomo.ieee.org
Subject: EMI guard bands


From: Cecil A. Gittens

I am in the process of putting a document together for products that are
tested for  Radiated  Conducted Emissions
that should have a Guard-band of 6 dB for FCC or CISPR22 class A or B.
Does it depend if the product is class A or B?
Does anyone have any pointers or suggestions?

Thanks.


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RE: emc for FDA

2001-12-03 Thread Jim Conrad

Brian,

For medical use 60601-1-2.  They prefer the 9-2001 version.

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of MCA Compliance
Sent: Saturday, December 01, 2001 12:53 PM
To: Emc-Pstc Post
Cc: Brian McAuliffe
Subject: emc for FDA


Do FDA specify their own EMC requirements/standards or do they use those of
the FCC (Part 15?) ?

Brian


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RE: FDA FCC

2001-10-30 Thread Jim Conrad

Jon,

If you look at Sec. 18.101  Basis and purpose, part 18 only applies to
medical equipment that emits
electromagnetic energy on frequencies within the radio frequency
spectrum in order to prevent harmful interference to authorized radio
communication services.  The Ultrasound equipment that I am familiar with
does not emit electromagnetic energy that would cause interference.  They
also comply with CISPR 11 class A or B emissions requirements depending on
where they are used.  Do you certify your Ultrasound equipment to Part 18?

Best regards,

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Jon Griver
Sent: Monday, October 29, 2001 8:20 AM
To: emc-p...@majordomo.ieee.org
Subject: FW: FDA  FCC


Jim,

Yes and no.

Yes. Medical ultrasound equipment is explicitly included in the scope of
Part 18 under Section 18.107(f). I assume the logic is that RF circuits are
required to generate the ultrasound.

No. Section 18.121 excludes non-consumer medical ultrasound equipment,
except for a few sections of Part 18 that deal mainly with allowed
frequencies.

Best Regards,

Jon Griver
http://www.601help.com - The Medical Device Developers' Guide to IEC 60601-1



 Jon,  Ultrasound equipment does us use RF directly to treat or diagnose
 patients.  I don't believe Ultrasound equipment falls under part 18.

 The FDA is now recommending the use of IEC 60601-1-2; 2001 for EMC.

 Best regards,

 Jim

 -Original Message-
 From: owner-emc-p...@majordomo.ieee.org
 [mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Jon Griver
 Sent: Sunday, October 28, 2001 2:07 AM
 To: emc-p...@majordomo.ieee.org
 Subject: FDA  FCC


 This is not quite the whole story.

 Medical devices must get FDA approval, including EMC aspects. However,
 medical equipment is also subject to FCC regulations.

 FCC Part 15 exempts medical equipment (Sec 15.103), though it is still
 subject to the general requirements of the FCC in that devices found to
 cause interference can be stopped from operating.

 Medical devices that intentionally use EM radiation are subject
 to FCC Part
 18. This includes ultrasound equipment, diathermy equipment, microwave
 therapeutic devices.

 Regards,

 Jon Griver
 http://www.601help.com - The Medical Device Developers' Guide to
 IEC 60601-1



 
  Hi,
 
  In the USA, it is the FDA.  For most medical products, the FDA
 determines
  that your product is Substantially Equivalent to a legally
  marketed device.
  This is the FDA 510(k) process.  They issue you a letter that
  allows you to
  legally market the device.
 
  For EMC, the FDA usually wants to see that you comply with IEC
  60601-1-2.
 
  Ned
 
 
  Ned Devine
  Program Manager III
  Entela, Inc.
  3033 Madison Ave. SE
  Grand Rapids, MI  49548
 
  616 248 9671 Phone
  616 574 9752 Fax
  ndev...@entela.com  e-mail
 
 
 
 
 
  -Original Message-
  From: am...@westin-emission.no [mailto:am...@westin-emission.no]
  Sent: Friday, October 26, 2001 5:15 AM
  To: emc-p...@majordomo.ieee.org
  Subject: FDA
 
 
 
  Hi all,
 
  What is the basic differences between FDA and FCC ? Don't laugh,
  yes I know
  it is a silly question, but if you want to certify medical
 equipment, are
  the requirements covered in the FDA or in the FCC regulations ?
 
  As you understand, within this field, I'm a really novice ...
 
  Best regards
  Amund Westin, Oslo/Norway
 
 
 
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RE: FDA FCC

2001-10-28 Thread Jim Conrad

Jon,  Ultrasound equipment does us use RF directly to treat or diagnose
patients.  I don't believe Ultrasound equipment falls under part 18.

The FDA is now recommending the use of IEC 60601-1-2; 2001 for EMC.

Best regards,

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Jon Griver
Sent: Sunday, October 28, 2001 2:07 AM
To: emc-p...@majordomo.ieee.org
Subject: FDA  FCC


This is not quite the whole story.

Medical devices must get FDA approval, including EMC aspects. However,
medical equipment is also subject to FCC regulations.

FCC Part 15 exempts medical equipment (Sec 15.103), though it is still
subject to the general requirements of the FCC in that devices found to
cause interference can be stopped from operating.

Medical devices that intentionally use EM radiation are subject to FCC Part
18. This includes ultrasound equipment, diathermy equipment, microwave
therapeutic devices.

Regards,

Jon Griver
http://www.601help.com - The Medical Device Developers' Guide to IEC 60601-1




 Hi,

 In the USA, it is the FDA.  For most medical products, the FDA determines
 that your product is Substantially Equivalent to a legally
 marketed device.
 This is the FDA 510(k) process.  They issue you a letter that
 allows you to
 legally market the device.

 For EMC, the FDA usually wants to see that you comply with IEC
 60601-1-2.

 Ned


 Ned Devine
 Program Manager III
 Entela, Inc.
 3033 Madison Ave. SE
 Grand Rapids, MI  49548

 616 248 9671 Phone
 616 574 9752 Fax
 ndev...@entela.com  e-mail





 -Original Message-
 From: am...@westin-emission.no [mailto:am...@westin-emission.no]
 Sent: Friday, October 26, 2001 5:15 AM
 To: emc-p...@majordomo.ieee.org
 Subject: FDA



 Hi all,

 What is the basic differences between FDA and FCC ? Don't laugh,
 yes I know
 it is a silly question, but if you want to certify medical equipment, are
 the requirements covered in the FDA or in the FCC regulations ?

 As you understand, within this field, I'm a really novice ...

 Best regards
 Amund Westin, Oslo/Norway



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RE: ESD - time between successive discharges

2001-08-02 Thread Jim Conrad

Just to give you an idea of how we handled this in 60601-1-2, we said: The
time between discharges shall have an initial value of 1 s. Longer time
between discharges may be required in order to be able to distinguish
between a response caused by a single discharge and a response caused by a
number of discharges.
That is, each discharge should be evaluated independently.  The time between
them must be considered based the type of equipment being tested.  Hope this
helps and is WG13's implementation of this problem.

Jim
-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Michael Hopkins
Sent: Thursday, August 02, 2001 6:48 AM
To: am...@westin.org; emc-p...@majordomo.ieee.org
Subject: Re: ESD - time between successive discharges


Seems to me the time between discharges is the same as the time between
pulses (I believe that was the intent). I don't have the standard in front
of me, but I think the max rate was 1/second, which means you could go
slower. In most tests I've seen, the several discharges at one point are run
at the 1/second rate, but then there could be several seconds or more
between the discharges at that point and the discharges at the next point.
At least one company actually runs tests at much higher discharge rates and
with many more shots/point than IEC recommends (the new draft of ANSI C63.16
goes to 50 shots/per point).

Michael Hopkins
Thermo KeyTek

- Original Message -
From: am...@westin.org
To: emc-p...@majordomo.ieee.org
Sent: Wednesday, August 01, 2001 4:06 PM
Subject: ESD - time between successive discharges



 Dear members,

 From IEC61000-4-2 and several EN-product standards, they specify the time
 between successive discharges to be at least 1 second.

 But what is the maximum time between each pulse ? I can not see that it is
 stated in any standards. I guess the test labs use 1 pulse pr second.

 I feel that the pulse rate can have influences on the EUT performance, so
1
 second compared to 3-5 seconds might be the difference between PASS and
FAIL.

 Any suggestions ?

 Best regards
 Amund Westin
 Oslo, Norway

 --
 Get your firstname@lastname email for FREE at http://Nameplanet.com/?su

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RE: Medical devices in Japan

2001-08-01 Thread Jim Conrad

Nick,

I have a contact in Japan if you need it.  I do know that Japan just
approved the 2nd Edition of IEC 60601-1-2 but what I am not sure of is if
JTA requires compliance or what the transition date might be.  If you would
like me to look into this, contact me directly.

Best regards,

Jim

Jim Conrad
Conrad EMC Consulting
P.O. Box 25
Hamilton, MA 01936  USA

Phone:  978-468-3909
E-Mail:  jc...@shore.net


-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Nick Williams
Sent: Tuesday, July 31, 2001 10:02 PM
To: emc-p...@majordomo.ieee.org
Subject: Medical devices in Japan


I've been asked if I know what the regime is for medical devices in
Japan. I don't know anything about this, but if there's anyone out
there who can give me a brief idea or possibly even some URLs to look
at, I'd be grateful.

Anyone in the business of providing consultancy in this area please
let me know and I'll likely put the enquirer in touch direct.

Thanks and regards

Nick.

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RE: Test Equipment ...

2001-08-01 Thread Jim Conrad
Just to add to Tania’s comment, all medical electrical equipment is exempt
from part 15.

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Tania Grant
Sent: Wednesday, August 01, 2001 12:16 AM
To: Doug McKean; EMC-PSTC Discussion Group
Subject: Re: Test Equipment ...

Doug, et al,

FCC Part 15 addresses digital devices only.   And they continue to use the
term digital over and over again.   The scope of FCC Part 15 does not
address analog devices, whether they be industrial, commercial, or medical
test equipment.  However, the FCC are exempting (and some say temporarily)
digital devices that are used exclusively as industrial, commercial, or
medical test equipment.   Therefore, no, a company that makes analog test
equipment does not have to EMC test such products.   (And someone tell me
please how exactly they would test them if they wanted to!)

taniagr...@msn.com mailto:taniagr...@msn.com

- Original Message -
From: Doug McKean
Sent: Tuesday, July 31, 2001 5:46 PM
To: EMC-PSTC Discussion Group
Subject: Re: Test Equipment ...


Price, Ed wrote:

 Doug:

 The rationale that I recall is that test equipment is expected to be
used by
 people who understand the nature of electrical measurements and
safety.
 These people will have the knowledge and resources, beyond those of
a
 typical consumer, to recognize and ameliorate interference and other
 problems. Further, it is argued that compliance measures might
hinder
 absolute accuracy and sensitivity of measurement equipment. Also,
that test
 equipment is not usually manufactured in numbers comparable to
typical
 consumer equipment, so the impact on a society is less.

 IIRC, there is a somewhat shorter and simpler explanation buried
somewhere
 in Part 15.

Okay, follow me on this for just a minute.

 47 CFR, 15.103, Exempted devices.
(c) A digital device used exclusively as industrial, commercial,
 or medical test equipment.

The important word is digital.  Why just digital?  Does this mean
if a company makes analog industrial, commercial, or medical test
equipment, that equipment MUST be tested?

Regards, Doug McKean  (slowly becoming more confused ...)



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RE: EN 61000-4-2 ESD Requirements

2001-08-01 Thread Jim Conrad

Hi Santo,

You didn't say what type of products you are making but for Medical
Electrical Equipment complying with the 2nd ED of 60601-1-2 it will be 8 kV
air and 6 kV contact.

Best regards,

Jim

-Original Message-
From: owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]On Behalf Of Sandy Mazzola
Sent: Tuesday, July 31, 2001 2:21 PM
To: emc-p...@ieee.org; emc-p...@majordomo.ieee.org
Subject: EN 61000-4-2 ESD Requirements

Members,

 Is there anyone who can let me know the status of  any forthcoming
increase in the EN 61000-4-2 ESD requirements of +/- 8  Kv air and +/- 4  Kv
contact.
Also any editorial comment on whether the current requirements are realistic
would also be appreciated.

Thanks
Have a  great day




Santo Mazzola
Regulatory Engineer
Symbol Technologies Inc
1 Symbol Plaza
Holtsville, N. Y. 11742-1300
Phone:  (631) 738-5373
Fax:  (631) 738-3318
E-mail: mazzo...@symbol.com



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RE: EN 55011 Fundamental ISM frequencies

2001-06-26 Thread Jim Conrad

Doug,

Doug asked:  Do the unrestricted limits for the ISM frequencies really apply
to both
radiated and conducted or to only radiated emissions?

I think yes and here is why.  The 2nd ED of 60601-1-2 required testing to
61000-4-6 at a level of 10V at the ISM frequencies below 80 MHz and 3V
everywhere else.  Hope this helps.

Best regards,

Jim

P.S.  I hope the main return path for the ISM transmitter is not back
through the power lines!

Jim Conrad
Conrad EMC Consulting
P.O. Box 25
Hamilton, MA 01936  USA

Phone:  978-468-3909
E-Mail:  jc...@shore.net


 -Original Message-
From:   owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]  On Behalf Of POWELL, DOUG
Sent:   Monday, June 25, 2001 7:21 PM
To: EMC-PSTC (E-mail)
Cc: HARDMAN, BRYAN; JOHNSON, J. D.
Subject:EN 55011 Fundamental ISM frequencies


Dear groups,

My company is a manufacturer of equipment defined in EN55011 (CISPR 11) as
Group 2, Class A products and a question has come up regarding the ISM
frequencies that I am hoping you can clarify for us.

Tables Ia and Ib of the standard list the fundamental ISM frequencies and
their associated limits (or lack of).  Since column 3 (column 2 of Ib) is
titled Maximum radiation limit, it has been thought by every compliance
engineer in my company, that these forgiveness bands only apply to radiated
emissions.  However, paragraph 3.3 states that ... The limits for terminal
voltages and radiation do not apply to these ISM frequencies ...

It appears that there is a discrepancy in the language if these two
references.

So the question is this:

Do the unrestricted limits for the ISM frequencies really apply to both
radiated and conducted or to only radiated emissions?

Any opinions or discussion on this would be greatly appreciated.


-doug


=
Douglas E. Powell
Regulatory Compliance Engineer
Advanced Energy Industries, Inc.
1625 Sharp Point Dr.
Ft. Collins, Co 80525

mailto:doug.pow...@aei.com
www.advanced-energy.com
=






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RE: Status of Frequency extension of EN 61000-4-3

2001-06-20 Thread Jim Conrad

FYI, IEC 60601-1-2: 2ED, EMC for Medical Electrical Equipment requires 3/10
V/m testing to 2.5 GHz!

Best regards,

Jim

 -Original Message-
From:   owner-emc-p...@majordomo.ieee.org
[mailto:owner-emc-p...@majordomo.ieee.org]  On Behalf Of Pettit, Ghery
Sent:   Monday, June 18, 2001 11:19 AM
To: 'Sandy Mazzola'; emc-p...@majordomo.ieee.org
Subject:RE: Status of Frequency extension of EN 61000-4-3


Sandy,

Whether or not IEC (or EN) 61000-4-3 has its applicable frequency range
extended, there is no effect on EN 55024:1998 or CISPR 24 until such time as
these documents are amended to increase the frequency range for the test.
As a member of CISPR SC G WG3, I can tell you that there is no proposal in
CISPR to increase the frequency range for this test in CISPR 24 at this
time.  Of course, we're meeting in Bristol, England next week and anything
could happen, but I don't expect this to come up.  Given the speed(?) with
which changes work their way through the system, it would be 2 or 3 years
before CISPR 24 could be amended if we started next week, then a 3 year
transition period in the EU, so if a successful effort to increase the
frequency range of this test were to start next week, you'd be looking at 5
to 6 years before it became mandatory in Europe.  Other countries using
CISPR 24 (Korea and Russia, for example) might act faster, but still nothing
could happen until CISPR 24 was amended and I would expect that to take 3
years.

Bottom line - don't start placing purchase orders for new equipment just
yet.

Ghery S. Pettit, NCE
Intel


-Original Message-
From: Sandy Mazzola [mailto:mazzo...@symbol.com]
Sent: Friday, June 15, 2001 8:04 AM
To: emc-p...@majordomo.ieee.org
Subject: Status of Frequency extension of EN 61000-4-3


To all,

My question pertains to EN 55024:1998,  Information Technology
Equipment-Immunity Characteristics,  flowing down to EN 61000-4-3 :1997,
Radiated Immunity.
   I am looking for the status of a frequency extension to EN 6100-4-3
radiated Immunity.  EN 61000-4-3:1997 lists 80 MHz to 1 GHz as the test
frequency range.
Is anyone aware of the Radiated Immunity requirements being extended
to 3 Ghz or  higher sometime in the near future.   If there are any drafts
proposing this can you list the draft number.
 Finally, if no present plans exist could anyone venture a prediction
for when and if the radiated Immunity frequency will be extended.

Thx

Sandy Mazzola

Santo Mazzola
Regulatory Engineer
Symbol Technologies Inc
1 Symbol Plaza
Holtsville, N. Y. 11742-1300
Phone:  (631) 738-5373
Fax:  (631) 738-3318
E-mail: mazzo...@symbol.com




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RE: New Immunity/ESD Specs.

2001-05-01 Thread Jim Conrad

IEC 61000-4-2 (2001-04) Consolidated Edition 1.2
https://domino.iec.ch/webstore/webstore.nsf/all/3391D5E5625356F8C1256A3B001
1096C?OpenDocument  – was just published by the IEC CO.

Best regards,

Jim

-Original Message-
From: owner-emc-p...@ieee.org [mailto:owner-emc-p...@ieee.org]On Behalf Of
John Juhasz
Sent: Monday, April 30, 2001 4:49 PM
To: 'emc-p...@ieee.org'
Subject: New Immunity/ESD Specs.

Hello all . . .
A 3rd party statement was made to me today about 'new' immunity
specifications for ITE. More specifically
for ESD.
I am currently using EN 50082-1:1997 for the immunity series, my ESD being
EN 61000-4-2:1995.
Is there anything newer going to be introduced any time soon?
Thanks
John Juhasz
Fiber Options
Bohemia, NY


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RE: Medical Directive

2001-04-30 Thread Jim Conrad

I don't think my first reply went out.  This a second try.  Sorry Cyril.

Best regards,

Jim


Cyril, Please see my answers to your questions below:

 -Original Message-
From:   owner-emc-p...@ieee.org [mailto:owner-emc-p...@ieee.org]  On Behalf
Of Binnom, Cyril A
Sent:   Friday, April 27, 2001 7:46 AM
To: emc-pstc
Subject:Medical Directive


Group:

I am attempting to send ITE equipment to the European Union, and the unit
will be used in a hospital environment. I have no problem testing to the
Medical or EMC Directive,  whichever is applicable, but I am in need of some
clarification

My questions are:

*   I have been told that if the unit is mobile, (which it is) then the
Medical Directive applies. There is no patient interface but it will be in a
hospital environment.

I your device does not have a PATIENT APPLIED PART, you do not have medical
electrical equipment and do not have to comply with 60601-1.  However, you
must ensure that it does not get used in the PATIENT vicinity, i.e. within
1.5 meters of the patient (see Figure 201 in IEC 60601-1-1)  You may have a
Medical System if this device attaches to Medical Electrical Equipment in
which case IEC 60601-1-1 will apply.  The software should comply with
60601-1-4.

*   Will EN 60601-1-2 (EMC) be upgraded in the near future
as I do not want to test to the current standard and have to go back in a
year or two and retest the unit, and if so is there a proposed standard for
review.

IEC 60601-1-2: Second edition will be published in July.  Completely new.
Uses 61000-4-XX for immunity.  New test levels.  Harmonics requirements.
Exclusion for ITE, etc.

*   Does the unit under EN 55011 have to be tested to Class B or Class A
limits for hospital use. I have been told that in Sweden and Germany, Class
B is mandatory.

The hospital environment is considered Class A.  Sweden has finally agreed.
Germany has always accepted Class A in the Hospital.  Check clause 4 of
CISPR 11.


*   A demo has been requested A.S.A.P. Does the demo have to be CE mark,
(it will not be sold) or is there room or a  clause that allows this one
unit to be shipped to the EU while compliance is being completed. I am under
the assumption, that the demo will be used in the hospital during this time.

You MUST have the CE mark if you plan to show it in an EU country.

Best regards,

Jim

Regards,

Cyril A. Binnom Jr.
EMI/EMC Approvals Engineer
LXE, Inc.
(770) 447-4224 Ext. 3240
(770) 447-6928 Fax
binno...@lxe.com









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Re: HP684XA harmonics analyser software

2001-03-01 Thread Jim Conrad
Hi Chris,

I spoke with Agilent in Rockaway a couple of weeks ago and they assured me they 
will be addressing A14 with a software update.  That is the good news.  
However, it will not be ready for another 4 -6 months!!!

Best regards,

Jim


Colgan, Chris wrote on 2/28/01 8:41 am:


Hi all

Does anyone know if Agilent have written a software upgrade (for A14 of 
EN61000-3-2) for their harmonics analysers yet?  The Agilent website won't tell 
and their contact link is broken.

Regards

Chris Colgan
Compliance Engineer
TAG McLaren Audio Ltd
The Summit, Latham Road
Huntingdon, Cambs, PE29 6ZU
*Tel: +44 (0)1480 415 627
*Fax: +44 (0)1480 52159
* Mailto:chris.col...@tagmclarenaudio.com  http://www.tagmclarenaudio.com



**  Please visit us 
at www.tagmclarenaudio.com
**

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intended recipient. If you receive this E-mail in error, please delete it from 
your system immediately and notify us either by E-mail, telephone or fax. You  
should not  copy, forward or otherwise disclose the content of the E-mail.

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The Summit, 11 Latham Road
Huntingdon, Cambs, PE29 6ZU
Telephone : 01480 415600 (+44 1480 415600) Facsimile : 01480 52159 (+44 1480 
52159)

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Re: IEC 606010-1-2

2001-01-27 Thread Jim Conrad
It is the same as 60601-1-2; 1993,  i.e. CISPR 11, class A or B depending on
the environment.

Best regards,

Jim


owner-emc-p...@ieee.org wrote on 1/25/01 2:34 pm:



Any advance info on conducted emissions for the new standard?

thnx
Brian O'Connell
Taiyo Yuden (USA), Inc.

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Jim Conrad
P.O. Box 25
Hamilton, M.A. 01936

Phone:  978-468-3909
attachment: winmail.dat

RE: EN61000-3-2 Amendments.

2001-01-12 Thread Jim Conrad

Al,

It relaxed the limits for almost all products except ITE, TV's, etc.  I do
not remember all the details since I have not had to apply it yet.
Essentially the harmonic current limits are no longer relative based on the
power consumption of the device but based are on absolute values as if the
product was drawing 15A(not sure of this exact #).   But essentially
anything will pass now.  You can purchase A14 on the IEC web site at
www.iec.chThere is also a 75 watt exemption.  Products less that 75
watts automatically comply.

Best regards,


Jim'


Jim Conrad
P.O. Box 25
Hamilton, MA 01936-0025
USA

jc...@shore.net
Phone #:  978-468-3909
FAX #: 978-468-3909


-Original Message-
From:   Allan, James [mailto:james_al...@milgo.com]
Sent:   Friday, January 12, 2001 2:53 PM
To: brett_sand...@snellwilcox.com; 'emc-pstc (E-mail)'; 'jc...@shore.net'
Subject:RE: EN61000-3-2 Amendments.

In a nutshell how did A14 change 61000-3-2.  I don't have a copy of
A14 yet.

Jim Allan
Manager, Engineering Services
Milgo Solutions LLC
1619 N Harrison Parkway
Sunrise, FL, 33323
E-mail james_al...@milgo.com
Phone (954) 846-3720
Fax (954) 846-5693

 -Original Message-
 From: Jim Conrad [SMTP:jc...@shore.net]
 Sent: Friday, January 12, 2001 10:09 AM
 To:   brett_sand...@snellwilcox.com; 'emc-pstc (E-mail)'
 Subject:  RE: EN61000-3-2 Amendments.


 Yes, you can use the A14 for the January 1, 2001 compliance.  Just be sure
 to add 61000-3-2 A14 to your DOC.

 Best regards,

 Jim

 Jim Conrad
 P.O. Box 25
 Hamilton, MA 01936-0025
 USA

 jc...@shore.net
 Phone #:  978-468-3909
 FAX #: 978-468-3909


 -Original Message-
 From: owner-emc-p...@ieee.org [mailto:owner-emc-p...@ieee.org] On Behalf
 Of
 brett_sand...@snellwilcox.com
 Sent: Friday, January 12, 2001 7:43 AM
 To:   emc-pstc (E-mail)
 Subject:  EN61000-3-2 Amendments.


 Does anybody know if the amendments made it into EN61000-3-2 for its
 January
 2001 compliance date?

  As a manufacturer of products that only use switch mode power supplies,
 the
 amendments are  of great importance to me.


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RE: EN61000-3-2 Amendments.

2001-01-12 Thread Jim Conrad

Yes, you can use the A14 for the January 1, 2001 compliance.  Just be sure
to add 61000-3-2 A14 to your DOC.

Best regards,

Jim

Jim Conrad
P.O. Box 25
Hamilton, MA 01936-0025
USA

jc...@shore.net
Phone #:  978-468-3909
FAX #: 978-468-3909


-Original Message-
From:   owner-emc-p...@ieee.org [mailto:owner-emc-p...@ieee.org] On Behalf Of
brett_sand...@snellwilcox.com
Sent:   Friday, January 12, 2001 7:43 AM
To: emc-pstc (E-mail)
Subject:EN61000-3-2 Amendments.


Does anybody know if the amendments made it into EN61000-3-2 for its January
2001 compliance date?

 As a manufacturer of products that only use switch mode power supplies,
the
amendments are  of great importance to me.


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RE: EN 61000-3-3 Flicker Tests

2000-12-05 Thread Jim Conrad

Gert, thanks for your reply.  I appreciate your reasoning on this matter as
I have just been thought similar reasoning on a standard I am working on,
IEC 60601-1-2, EMC for Medical electrical equipment.  The group responsible
for writing IEC 61000-3-2, IEC SC 77A WG 1, has agreed with our
interpretation of  public low voltage distribution systems, that is, it is
the same as CISPR 11 Class A environment, Class A equipment is equipment
suitable for use in all establishments other than domestic and those
directly connected to a low voltage power supply network which supplies
buildings used for domestic purposes.  However, as you mentioned, these
standard are subject to change and my understanding is that both harmonics
and flicker requirements will apply to all environments in the future.  I
hope this helps.

Jim


Jim Conrad
P.O. Box 25
Hamilton, MA 01936-0025
USA

jc...@shore.net
Phone #:  978-468-3909
FAX #: 978-468-3909


-Original Message-
From:   CE-test - Ing. Gert Gremmen - ce-marking and more...
[mailto:cet...@cetest.nl]
Sent:   Monday, December 04, 2000 1:18 PM
To: Jim Conrad; bfag...@us.tuv.com; emc-p...@ieee.org
Subject:RE: EN 61000-3-3 Flicker Tests

  File: Gert Gremmen.vcf 
be careful Jim,

In Europe one harmonic standard has no power to exclude
the requirements of another harmonic standard that is applicable to the
apparatus.
Especially those of EN 61000-3-2 and 61000-3-3  !!
The target of the EMC-directive is covering all essential EMC requirements:

-Low frequency
-High frequency
-Radiated
-Conducted
for
-Emission
-Immunity
and the permutations of the above.
This does not mean that testing is required; you just sign for
compliance. Any proof of compliance, even reasoning may be sufficient.
In some cases you will need the opinion of a third party (CB).

As some harmonized standards (55011) are older than these requirements, some
incompatible statements may occur. These will be ruled out slowly when newer
versions
of the standard appear. Normally every standard will be updated once every 4
years.

Be especially careful with all exceptions and notes in standards that
for some (not) obvious reason try to exclude certain categories of
equipment from some difficult to meet requirements IF a such-and-so-note
is printed on the equipment. These have no value in Europe for ce marking.

Basically most Class A (EN 55022 and 55011) are not easy to be sold in
Europe due to the very strict definition of heavy industrial environment.

In fact, if there is no very stringent (functional) reason why an equipment
cannot meet
Class B emissions, it should. No clauses allowed 

Regards,

Gert Gremmen, (Ing)

ce-test, qualified testing

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


-Original Message-
From: owner-emc-p...@ieee.org [mailto:owner-emc-p...@ieee.org]On Behalf
Of Jim Conrad
Sent: Monday, December 04, 2000 3:17 PM
To: bfag...@us.tuv.com; emc-p...@ieee.org
Subject: RE: EN 61000-3-3 Flicker Tests



Hi Bruce,

Your customer is correct.  If the device is classified as a Class A
(according to CISPR 11), you do not need to comply with flicker
requirements.

Jim


Jim Conrad
P.O. Box 25
Hamilton, MA 01936-0025
USA

jc...@shore.net
Phone #:  978-468-3909
FAX #: 978-468-3909


-Original Message-
From: owner-emc-p...@ieee.org [mailto:owner-emc-p...@ieee.org] On
Behalf Of
bfag...@us.tuv.com
Sent: Sunday, December 03, 2000 6:04 PM
To:   emc-p...@ieee.org
Subject:  EN 61000-3-3 Flicker Tests


Hello group!

I've got a customer in our EMC lab that makes a laboratory instrument
incorporating heaters with a typical 3-4 amp input current at 230vac.  He
is failing the flicker test due to the design of the heater control.  They
are undertaking a redesign but would like to keep selling product in the
interim.

They have come up with an interesting interpretation of the scope of EN
61000-3-3:  the standard specifies that the tests are applicable to
products connected to the public low voltage distribution
systems  but if
you take a typical industrial location or even a typical commercial
location, isn't it true that these locations are fed by a dedicated
transformer at the building that isolates them from the public network?  I
guess the question becomes - what is considered the public network?  What
if the marketing of the product was restricted to industrial locations?

My initial reaction to the question was that anyplace you can plug or wire
into at typical 230vac is considered the public network, especially
considering the mixed residential / commercial buildings common in Europe.

Anyone care to comment?

Bruce Fagley
Sr. Specialist, EMC
Industrial Products
TUV Rheinland
12 Commerce Rd.
Newtown CT. 06470
203-426-0888 ext 119
203-426-4009 fax

RE: EN 61000-3-3 Flicker Tests

2000-12-04 Thread Jim Conrad

Hi Bruce,

Your customer is correct.  If the device is classified as a Class A
(according to CISPR 11), you do not need to comply with flicker
requirements.

Jim


Jim Conrad
P.O. Box 25
Hamilton, MA 01936-0025
USA

jc...@shore.net
Phone #:  978-468-3909
FAX #: 978-468-3909


-Original Message-
From:   owner-emc-p...@ieee.org [mailto:owner-emc-p...@ieee.org] On Behalf Of
bfag...@us.tuv.com
Sent:   Sunday, December 03, 2000 6:04 PM
To: emc-p...@ieee.org
Subject:EN 61000-3-3 Flicker Tests


Hello group!

I've got a customer in our EMC lab that makes a laboratory instrument
incorporating heaters with a typical 3-4 amp input current at 230vac.  He
is failing the flicker test due to the design of the heater control.  They
are undertaking a redesign but would like to keep selling product in the
interim.

They have come up with an interesting interpretation of the scope of EN
61000-3-3:  the standard specifies that the tests are applicable to
products connected to the public low voltage distribution systems  but if
you take a typical industrial location or even a typical commercial
location, isn't it true that these locations are fed by a dedicated
transformer at the building that isolates them from the public network?  I
guess the question becomes - what is considered the public network?  What
if the marketing of the product was restricted to industrial locations?

My initial reaction to the question was that anyplace you can plug or wire
into at typical 230vac is considered the public network, especially
considering the mixed residential / commercial buildings common in Europe.

Anyone care to comment?

Bruce Fagley
Sr. Specialist, EMC
Industrial Products
TUV Rheinland
12 Commerce Rd.
Newtown CT. 06470
203-426-0888 ext 119
203-426-4009 fax


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 Richard Nute:   ri...@ieee.org




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