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The manufacturer below hereby declares that the medical device, or the Technical
documentation, specified in this User Manual is Dual marked for sale on both the UK
and EU markets. The Class I Medical Device covered by this User Manual complies
with the General Safety and Performance
Requirements within Annex-1 of EC Regulation 2017/745
Registered Office:
Ferno (UK) Limited
Ferno House, Stubs Beck Lane, Cleckheaton, West Yorkshire, England. BD19 4TZ
Tel: + 44 (0) 1274 851999
Email:
services@ferno.co.uk
/
sales@ferno.co.uk
www.ferno.co.uk
Registered number: 1007475 England
As our policy is one of continuous development Ferno (UK) Ltd reserves the right to change the specifications without notice.
Stock Code: 2003-0076
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