Medisafe PCF Pro, User Manual

Page: 16 / 74

PCF Pro User Manual
DOC01851 Page 16 of 74
Compliance
The PCF Pro has been designed to perform
within the guidelines recommended by
international decontamination Standards. A
stringent quality control program ensures that
every unit is manufactured and tested under
controlled conditions to ensure that all
products perform identically.
Commitment to RoHS and WEEE
Requirements
Medisafe is committed to meeting or
exceeding the requirements of the RoHS CE
Marking directive (2011/65/EC) ( Restriction of
the Use of Certain Hazardous Substances in
Electrical and Electronic Equipment
).
Medisafe is also committed to meeting all
requirements of the WEEE directive
(2012/16/EU) (
Waste Electrical and Electronic
Equipment ).
WEEE and Battery Disposal
Waste electrical and electronic
products must not be placed in the
general refuse but collected
separately. Separately collected
WEEE products are to be sent to an approved
recycling or disposal operators for safe
recycling, recovery or reuse.
Medisafe UK Ltd is registered with the "B2B
Compliance" Scheme. B2B Compliance on
behalf of Medisafe, takes on the legal
responsibilities of the reporting, collection and
treatment of, all WEEE that Medisafe UK Ltd is
obligated for - and ensures that the
appropriate recycling targets are met. .For
independent confirmation of Medisafe UK Ltd
status can call B2B Compliance on 0845 680
9829 or visit www.b2bcompliance.org.uk
.
To fulfil our B2B WEEE take-back obligations,
B2B Compliance will undertake the
appropriate collection and disposal of
obligated products of Medisafe UK Ltd.
If a Medisafe Product has reached its end of
life, please contact B2B Compliance
collections team on 0845 680 9829 or
collections@b2bcompliance.org.uk to arrange
collection and treatment.
Otherwise, please recycle where facilities
exist. Check with your Local Authority or
Distributor for recycling advice.
Declaration of CE Conformity
The PCF Pro is designed and manufactured in
the UK by Medisafe UK Ltd. and complies with
the essential requirements of the Medical
Devices Directive 93/42/ EEC (where
appropriate). All products are CE compliant
and are registered as Class IIb devices
through the application of rule 15 within Annex
IX of the Medical Devices Directive 93/42/
EEC.
Product Identity
The model and serial number label are located
on the inside panel of the chemical
compartment.
Example of serial number label:
The software version is shown on the front
panel display when the unit is first switched on.
Manufacturer Information
Medisafe UK Ltd
Unit 1 Twyford Industrial Estate
Twyford Road
Bishop’s Stortford
Hertfordshire CM23 3LJ
England
Tel.: +44 (0) 1279 461641
Fax: +44 (0) 1279 461643
E-mail
info@medisafeinternational.com