Hello Jon,

Thanks for the clarification. This helps in understanding which safety 
standards may be applied to a medical device based on its intended use. 
Therefore, it is very important that we understand what a medical device is 
versus medical equipment or laboratory equipment, as they are defined by 
regulatory authorities and standards development organizations. 
Unfortunately, we may use medical device and medical equipment 
interchangeably and unintentionally confuse people, just like I did.

Best regards,
Ron Wellman

At 06:58 PM 2/20/2003 +0200, Jon Griver wrote:

>Ron,
>
>Classification of in-vitro devices as medical equipment, requiring 
>regulatory approval, does not
>influence the choice of product safety standard to be used. If it does not 
>fall within the scope of
>IEC 60601-1, and is only used in the lab, then IEC 61010 should be used, 
>though IEC 60950 would
>probably be acceptable if the instrument is based on a PC.
>
>Regards,
>
>Jon Griver
>http://www.601help.com
>The Medical Device Developers Guide to IEC 60601-1
>
>
>Hello Greg,
>
>I have to disagree with your interpretation. There are many in vitro
>devices that are classified as medical equipment and are subject to
>pre-market approvals in the US, Japan, and EU. There are strict regulations
>on labeling products in the US where even advertising is considered
>labeling. It's not as simple as contacting a live human, there are many
>other factors involved based on regulations and interpretations of
>regulatory authorities.
>
>Best regards,
>Ron Wellman
>
>At 11:15 PM 2/19/2003 -0500, Gregg Kervill wrote:
>
> >Does it contact a live human - if answer no - it is not medical equipment.
> >
> >The purpose for the medical device directive is to protect people for harm
> >or infection - being alive would seem to be essential for this.
> >
> >G
> >
> >
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