You will receive hundreds of opinions - none will be correct; all will be
correct. For the 3d edition of 60601-1, if you can justify the use of
ITE-certified equipment in the RMF, go for it...

For the U.S., there may be some problems with the FDA, as there is a
disjoint between the 2d edition and adoption of 3d edition.

Brian

-----Original Message-----
From: emc-p...@ieee.org [mailto:emc-p...@ieee.org]On Behalf Of McInturff,
Gary
Sent: Thursday, October 20, 2011 11:21 AM
To: 'EMC-PSTC@LISTSERV.IEEE.ORG'
Subject: Medical equipment versus ITE equipment used in medical facilities

List members,
          I've been looking over the medical directive or at least summaries
of it, and EN60601-1 trying to determine what requirements would say that a
general purpose keyboard must be evaluated or identified as a medical device
or a part of a medical device.
          The keyboard is designed with bacterial contamination and cleaning
in mind. It is completely sealed - not just a cover added over an existing
keyboard - and resistant to typical clearers and chemicals use in hospitals.
But other than that it's a standard qwerty keyboard with a USB connection to
a host. For data collection etc. Typical usage can be at a nurses station or
in a patient room as part of a patient records systems. But there is no
designed function to specifically help out with patient treatment systems
like cat scanners, infusion pumps et al.
          I suppose there is nothing to prevent one of these system with a
USB port to plug in the keyboard.
          Can someone point me in the direction of the relevant documents
that would describe when an ITE item used in a medical environment is
required to be evaluated as a medical device.

-
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