But there are products meeting that definition of machine that are covered by 
the LVD and specifically excluded from the  MD:

— household appliances intended for domestic use,
— information technology equipment,
— ordinary office machinery,

-Dave

From: Douglas Nix [mailto:[email protected]]
Sent: Thursday, March 30, 2017 5:20 PM
To: [email protected]
Subject: Re: [PSES] MD vs LVD for Laboratory Equipment

I concur with Michael Loerzer. IMO, the test labs didn’t feel comfortable doing 
MD evaluations, so they used the “out” that was in the text of the previous MD 
(98/37/EC) that said that if the hazards were ‘predominantly electrical in 
nature” then the MD needn’t apply. Many machines were “slid-past” based on this 
misuse of the text of the MD, which is why the text was changed in the 2006 
edition.

If the device is “an assembly of linked parts, at least one of which moves” 
it’s a machine.
--
Doug Nix
[email protected]<mailto:[email protected]>

“Scientists investigate that which already is; Engineers create that which has 
never been.” - Albert Einstein



On 30-Mar-17, at 17:03, Kunde, Brian 
<[email protected]<mailto:[email protected]>> wrote:

Michael,

That sounds great.

I have emails from the TUV:Rheinland inspector who presented his position on 
the Cut-off Saw he evaluated to why it should be declared under the LVD and not 
the MD. I can send you those emails if you think that would be helpful.

Looking forward to hearing more from you. Sorry if do not always use the 
correct wording or terminology. We are a relatively small company and don’t 
have people sitting on committees or attending meetings on these topics. We 
must rely on others, such as what consultants tell us, what we read in 
publications, from test reports and what test labs tell us, field inspectors, 
what our customers expect, and what our competitors are doing.  When these 
sources start doing things that are different from what we are doing, it is my 
job to try and figure out why.

Thanks so much for your help with this.

Brian


From: [email protected]<mailto:[email protected]> 
[mailto:[email protected]]
Sent: Thursday, March 30, 2017 4:23 PM
To: Kunde, Brian; [email protected]<mailto:[email protected]>
Subject: AW: [PSES] MD vs LVD for Laboratory Equipment

Second comment: on 8th of May, 2017 I have a meeting with the responsible 
market surveillance authority in Baden-Wuerttemberg regarding our experiences, 
“blooper” and open questions of manufacturers/importers. If you like I can 
discuss  your “story/experiences” with these officials because one of the 
participants is the German representative for the MD in Brussels.

Michael

Von: Kunde, Brian [mailto:[email protected]]
Gesendet: Donnerstag, 30. März 2017 20:19
An: [email protected]<mailto:[email protected]>
Betreff: [PSES] MD vs LVD for Laboratory Equipment

Sorry to say, this issue has once again reared its ugly head. I appreciate any 
and all input.

History: For many many years, laboratory equipment fell under the Low Voltage 
Directive (LVD), even products with moving parts. It was specifically excluded 
from the Machinery Directive (MD). The Safety Standard for Laboratory Equipment 
EN 61010-1 is harmonized to the LVD.  Life was good.

Then a new version of the MD was released which did not exclude Laboratory 
Equipment. Many of the EHSR from annex I did not apply and there were no 
harmonized standards specific to laboratory equipment. So the same set of 
safety rules that apply to Industrial/Factory Machinery must somehow be applied 
to Carbon Analyzers, Calorimeters, Hardness Testers, and Mass Spectrometers. 
Life sucks.

BUT then the New Safety Standards EN 61010-1 3rd Ed. was released which 
included hazards from Moving Parts and referenced a Risk Assessment for any 
hazards not covered by the standard.  The standard now covered all hazardous 
conditions associated with Laboratory Equipment including moving parts, 
electrical, chemical, hot/cold temperatures, radiation, pressurized fluids, 
everything. AND THEN the new LVD was released which was aligned with the NLF.  
Can Life be Good Again?

The Topper:  Recently we have been contacted by two different Notified Bodies 
in Europe which has informed us that we should be using the LVD and not the MD. 
 When I asked for a reason why they basically said what I just typed above.  
One NB lab in Italy just performed a Safety Evaluation on one of our Cut-Off 
Saws (considered a prep machine for scientific analysis) and they evaluated it 
to the EN 61010-1:2010 and the LVD.  When I questioned this and inquired about 
the MD, they argued that the LVD and EN 61010-1 NOW covers all hazards assessed 
within the product and the MD would not be the appropriate Directive.

We have also started to see several of our business partners (companies we work 
with to produce buy/sell options and laboratory peripherals with moving parts 
like sample loaders)  declaring compliance to the LVD instead of the MD.  As 
first I tried to correct them but then they sent us test reports from NB labs 
in Europe evaluating their products to the LVD.  Whodathunkit?

However, I checked with the TUV:SUD lab we use here in the states and they are 
still saying that the MD is the correct directive to use.  Ok, now I’m 
officially confused.

So, has it officially changed? Or is it changing? Can manufacturers of 
laboratory equipment go back to declaring compliance to the LVD even if their 
products have moving parts?  Has anyone seen any official new releases, 
articles, decisions, on this topic?  Does anyone want to research and write an 
Article on this topic?

Is there an official authority who can once and for all settle this topic of 
continuing conflict, nightmares, and ulcers?

Thanks for your time.
The Other Brian


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