10
Liability
The manufacturer recommends using the device only under the specified conditions and for
the intended purposes. The device must be maintained according to the instructions for use
supplied with the device. The manufacturer is not liable for any adverse outcome caused by any
component combinations that were not authorized by them.
CE Conformity
This product meets the requirements of the European Regulation EU 2017/745 for medical
devices. This product has been classified as a class I device according to the classification rules
outlined in Annex VIII of the regulation. The EU declaration of conformity certificate is available at
the following internet address:
Warranty
This device warranted for 6 months.
The user should be aware that changes or modifications not expressly approved could void the
warranty, operating licenses, and exemptions.
See the Blatchford website for the current full warranty statement.
Reporting of Serious Incidents
In the unlikely event of a serious incident occurring in relation to this device it should be
reported to the manufacturer and your national competent authority.
Environmental Aspects
This product is fabricated from silicone rubber and fabric that cannot be easily recycled: please
dispose of it responsibly as general waste, as per local waste handling regulations.
938399PK1/1-0521
Medical Device
Single Patient – multiple use
Manufacturer’s Registered Address
Blatchford Products Limited, Lister Road, Basingstoke RG22 4AH, UK.
Trademark Acknowledgements
Silcare Breathe and Blatchford are registered trademarks of Blatchford Products Limited.
Summary of Contents for Silcare Breathe SBTTLP Series
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