System information

System Information
Vicon MX Hardware System Reference xix
CE Declaration of Conformity
Electromagnetic Compatibility as defined by
the EMC Directive 89/336/EEC of the 1st of January, 1992
We, Vicon Motion Systems Limited
Unit 14 Minns Estate
Oxford OX2 0JB
United Kingdom
declare that to the best of our knowledge that the Vicon MX motion capture system
manufactured by Vicon Motion Systems Limited meets the intent of the Medical Devices
Directive 93/42/EEC for Class 1 products in that it satisfies:
• The intent of EC Directive 89/336/EEC for electromagnetic compatibility
compliance as listed in the official journal of the European Communities.
• The essential safety requirements as detailed in Directive 73/23/EEC, including
Article 13 of the Official Journal of the European Communities L220 Volume 36
dated 30
th
August 1993 amending Directive 73/23/EEC.
Vicon Motion Systems Limited has tested and demonstrated that all products of its own
manufacture meet:
Emissions to:
EN55022:1998 Conducted, Class A
EN55022:1998 Radiated, Class B
Immunity to:
EN55024:1998 (EN61000-3-2: 2000 and (EN61000-3-3: 1995)
Low Voltage Directive to:
EN60950:2000
The equipment has been designed to meet CEI IEC 601-1-1 where applicable for a Class
1 device (Para 2.2.4). Not for use in an operating theater or anesthetic gas
environment.
T.M.L. Shannon, FIE Aust, CPEng (BIOMED), FRSA
Director of Operations
10 August 2006
MXhardware_Reference.book Page xix Thursday, September 7, 2006 11:36 AM