I agree with everything Charlie says. 

Try talking to some Machinery Notified Bodies instead of ex-LVD Notified 
Bodies. 

Happy to help further if you want to contact me directly. 

Nick. 


> On 30 Mar 2017, at 20:22, Charlie Blackham <[email protected]> 
> wrote:
> 
> Brian
>  
> Few comments:
> The scope of the Directive determines applicability, not the scope of the 
> standards – standards are just a way of demonstrating compliance with 
> Directives, which are law (when transposed in national legislation). 
> Directive comes first, standard a distant second.
> There aren’t any Notified Bodies to the LVD, (check here 
> <http://ec.europa.eu/growth/tools-databases/nando/index.cfm?fuseaction=directive.main>),
>  so all you are getting is a report from a lab that is accredited against a 
> standard, and an accredited report is not a 100% guarantee that the correct 
> thing has been done.
> The manufacturer is always legally responsible
> “But sir, that’s what they do” is not a legal defence I’d recommend :)
> You can apply any standards you wish to support compliance to the MD – 
> there’s nothing to stop you using EN61010-1 for clause 1.5.1 (and probably a 
> few others)
> The LVD update was just an NLF alignment for market enforcement, and did not 
> change its scope
> Machinery Directive Notified Bodies only really deal with Annex IV
>  
>  
> My view is:
> The application of the Machinery Annex I EHSRs to something that is not very 
> “machine like” shouldn’t be too onerous
> If in doubt, applying the MD instead of the LVD would only mean that you may 
> have done too much, so would always be a defensible position, the reverse is 
> not true.
>  
> Regards
> Charlie
>  
> Charlie Blackham
> Sulis Consultants Ltd
> Tel: +44 (0)7946 624317
> Web: www.sulisconsultants.com 
> <https://outlook.hslive.net/owa/redir.aspx?C=02be3bf3e3a544d1bdf7b6c99fbd12f5&URL=http%3a%2f%2fwww.sulisconsultants.com%2f>
> Registered in England and Wales, number 05466247
>  
> From: Kunde, Brian [mailto:[email protected] 
> <mailto:[email protected]>] 
> Sent: 30 March 2017 19:19
> To: [email protected] <mailto:[email protected]>
> Subject: [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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