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This topic provides information relating to the EU Declaration of Conformity (Vicon MX T-Series).

Conformity of the Metrological Performance of CLASS 1 Products in accordance with


VII, Section 5 of the Medical Devices Directive 93/42/EEC


of 14th June 1993.
Aas amended by


EU Council Directive 2007/47/EC of 5th September 2007.

We, Vicon Motion Systems Limited
Unit 6, Oxford Industrial Park
Mead Road, Yarnton, Oxford, OX5 1QU

declare that the VICON MX T-Series Cameras (including Bonita and Bonita 2), Active Wand and Giganet as a support part of a supplied T-Series motion capture system Gait Analysis System manufactured by VICON MOTION SYSTEMS LIMITED has been tested prior to shipment and meets the following metrological performance:


Measurement Criteria

  • Supporting software Nexus 2.10 or later, Shogun 1.4 or later, Tracker 3.8 or later.
  • Using a minimum of four cameras, resolution of the distance between the centers of two static 14 mm spherical markers located within a volume no less than 4 m x 4 m x 1.5 m to within 1 mm Mean; 1 mm Standard Deviation; sample size no less than 1,000.Resolution of a given analog voltage to within +/-20 mV RMS within the following configurations and constraints:
  • No fewer than two cameras of any variant fully viewing static markers
  • Independent of lens and strobe variants fitted to each camera
  • Controlled lighting (no greater than 100 lux) and temperature (17-25° C)
  • Single termination to each analog input
  • Testing using the following Vicon application software: Nexus Version 1.4 or later

Analogue Digital Conversion

Resolution to ± 10 mV mean and ± 10 mV (1 Standard Deviation).


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