TensCare unifit Instrucciones De Uso página 28

European Medical Device Regulation
requires that any serious incident that
has occurred in relation to this device
should be reported to the manufacturer
and the competent authority in your
country. This can be found at:
h t t p s : // e c . e u r o p a . e u / d o c s r o o m /
d o c u m e n t s /3 6 6 8 3/a t t a c h m e n t s / 1 /
translations/en/renditions/pdf
16. EMC
Wireless communications
such as wireless home network devices,
mobile phones, cordless telephones and
their base stations, walkie-talkies can
affect this equipment and should be
used no closer than 30cm (12 inches) to
any part of the device.
(Note. As indicated in 5.2.1.1(f) of IEC 60601-
1-2:2014 for ME EQUIPMENT).
Note: For hospital use, full EMC
advice tables are available on
request.
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17.
One of the provisions of the European
Directive 2012/19/EU is that anything
electrical or electronic should not be
treated as domestic waste and simply
thrown away. To remind you of this
Directive all affected products are now
equipment
being marked with a crossed-out wheelie
bin symbol, as depicted below.
To comply with the Directive, you can
return your old electro-therapy unit to
us for disposal. Simply print a postage-
paid PACKETPOST RETURNS label from
our website www.tenscare.co.uk, attach
this to an envelope or padded bag with
the unit enclosed, and post it back to us.
Upon receipt, we will process your old
device for components recovery and
recycling to help conserve the world's
resources and minimise adverse effects
on the environment.
Disposal
of Electronic
Products
(WEEE)