The following information relates to the Medical Devices Directive:
EU Declaration of Conformity (Vicon Vero)
0088
Medical Devices Directive 93/42/EEC as amended by
EU Council Directive 2007/47/EC of 5th September 2007.
Electromagnetic Compatibility to EMC Directive 2014/30/EU
Electrical Safety to Low Voltage Directive 2014/35/EU.
We, Vicon Motion Systems Limited
Unit 6, Oxford Industrial Park
Mead Road, Yarnton, Oxford, OX5 1QU
UNITED KINGDOM
declare that the VICON VERO Cameras manufactured by VICON MOTION SYSTEMS LIMITED meet ANNEX V and VII Section 5 of the Medical Devices Directive 93/42/EEC as amended by Directive 2007/47/EC in that the Quality Management System has been approved by Lloyd’s Register Quality Assurance, a notified body of the European Union (Reg No. 0088) for the manufacture and support of the aforementioned CLASS 1(m) Medical device. Product configurations and software options (Vicon Vero cameras), detail the product configurations and software options that conform to the metrological requirements of the Directive.
This declaration of conformity is issued under the sole responsibility of the manufacturer.
VICON MOTION SYSTEMS LIMITED has tested and demonstrated that all products of its own manufacture meet 2014/30/EU:
Electromagnetic Compatibility to:
EN60601-1-2:2007
General Requirements for Safety to:
Vero Cameras EN60601-1:2006 + A12:2014
Network Hub UL60950–1, 2nd Edition
Thomas Shannon, TD PhD FIE (Aust), CPEng (Biomed.)
Director of Compliance
22 November 2017
Not for use in an operating theater, anesthetic gas environment, or oxygen-rich environments. Not for use where there is a risk of compromising the essential performance of medical electrical equipment. Not suitable for use in high magnetic flux, ionizing radiation, dust ingress, high vibration, sterile, or life- or safety-critical environments.
Product configurations and software options (Vicon Vero)
This topic provides information relating to the EU Declaration of Conformity (Vicon Vero cameras).
Conformity of the Metrological Performance of CLASS 1 Products Manufactured in Accordance with
Annex VII, Section 5 of the Medical Devices Directive 93/42/EEC of the 14th June 1993.
As 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
UNITED KINGDOM
declare that the VICON VERO Cameras manufactured by VICON MOTION SYSTEMS LIMITED have been tested prior to shipment and meet the following metrological performance:
Measurement criteria
- Supporting software Blade 3.4 or later, Nexus 2.4 or later, and Tracker 3.3 or later.
- 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.
CE Declaration of Conformity (Vicon Vantage)
0088
Medical Devices Directive 93/42/EEC as amended by Directive 2007/47/EC.
Electromagnetic Compatability to EMC Directive 2004/108/EC.
Electrical Safety to Low Voltage Directive 2006/95/EC.
We, Vicon Motion Systems Limited
Unit 6, Oxford Industrial Park
Mead Road, Yarnton, Oxford, OX5 1QU
UNITED KINGDOM
declare that the VICON VANTAGE Cameras manufactured by VICON MOTION SYSTEMS LIMITED meets ANNEX V and VII Section 5 of the Medical Devices Directive 93/42/EEC as amended by Directive 2007/47/EC in that the Quality Management System has been approved by Lloyd’s Register Quality Assurance, a notified body of the European Union (Reg No. 0088) for the manufacture and support of the aforementioned CLASS 1(m) Medical device. Product configurations and software options (Vicon Vantage cameras) detail the product configurations and software options that conform to the metrological requirements of the Directive.
VICON MOTION SYSTEMS LIMITED has tested and demonstrated that all products of its own manufacture meet 2004/108/EC:
Electromagnetic Compatibility to:
EN60601-1-2:2007
General Requirements for Safety to:
Vantage Cameras EN60601-1:2006 + A12:2014
Network Hub UL60950–1, 2nd Edition
Thomas Shannon, TD PhD FIE (Aust), CPEng (Biomed.)
Director of Compliance
22 November 2017
Not for use in an operating theater, anesthetic gas environment, or oxygen-rich environments. Not for use where there is a risk of compromising the essential performance of medical electrical equipment. Not suitable for use in high magnetic flux, ionizing radiation, dust ingress, high vibration, sterile, or life- or safety-critical environments.
Product configurations and software options (Vicon Vantage)
This topic provides information relating to the CE Declaration of Conformity (Vicon Vantage cameras).
Conformity of the Metrological Performance of CLASS 1 Products Manufactured in Accordance with
Annex V and VII, Section 5 of the Medical Devices Directive 93/42/EEC of 14th June 1993.
As 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
UNITED KINGDOM
declare that the VICON VANTAGE Cameras manufactured by VICON MOTION SYSTEMS LIMITED have been tested prior to shipment and meet the following metrological performance:
Measurement criteria
- Supporting software Blade 3.2 or later, Nexus 2.2 or later, and Tracker 3.1 or later.
- 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.
CE Declaration of Conformity (Vicon MX T-Series)
0088
Medical Devices Directive 93/42/EEC as amended by Directive 2007/47/EC.
Electromagnetic Compatability to EMC Directive 2004/108/EC.
Electrical Safety to Low Voltage Directive 2006/95/EC.
We, Vicon Motion Systems Limited
Unit 6, Oxford Industrial Park
Mead Road, Yarnton, Oxford, OX5 1QU
UNITED KINGDOM
declare that the VICON MX T-Series motion capture system manufactured by VICON MOTION SYSTEMS LIMITED meets ANNEX V and VII Section 5 of the Medical Devices Directive 93/42/EEC as amended by Directive 2007/47/EC in that the Quality Management System has been approved by Lloyd’s Register Quality Assurance, a notified body of the European Union (Reg No. 0088) for the manufacture and support of the aforementioned CLASS 1 Medical device. Product configurations and software options (Vicon MX T-Series), details the product configurations and software options that conform to the metrological requirements of the Directive.
VICON MOTION SYSTEMS LIMITED has tested and demonstrated that all products of its own manufacture meet 2004/108/EC: MX T-Series Systems (MX Giganet based)
Electromagnetic Compatibility to:
EN60601-1-2:2007
Immunity to paragraph 6.2.3.1 to:
Immunity test level of 3V/m over 50 - 60 Hz
Electrical Safety of MxGiganet Power Supply Unit (Low Voltage Directive 2006/95/EC)
IEC 60601-1:1:1988 + A1:1991 + A2:1995 EN 60601-1:1990 A1,A2 and A13, excluding clause 36 and Korean national differences.
T.M.L. Shannon, TD, FIE (Aust), CPEng (Biomedical)
Director of Regulatory Compliance
22 November 2017
Not for use in an operating theater, anesthetic gas environment, or oxygen-rich environments. Not for use where there is a risk of compromising the essential performance of medical electrical equipment. Not suitable for use in high magnetic flux, ionizing radiation, sterile, or life- or safety-critical environments.
Product configurations and software options (Vicon MX T-Series)
This topic provides information relating to the CE Declaration of Conformity (Vicon MX T-Series).
Conformity of the Metrological Performance of CLASS 1 Products in accordance with
Annex V and VII Section 5 of the Medical Devices Directive 93/42/EEC as amended by
Directive 2007/47/EC
We, Vicon Motion Systems Limited
Unit 6, Oxford Industrial Park
Mead Road, Yarnton, Oxford, OX5 1QU
UNITED KINGDOM
declare that the VICON MX T-Series motion capture system manufactured by VICON MOTION SYSTEMS LIMITED has been tested prior to shipment and meets the following metrological performance:
- 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
