Vicon® is a registered trademark of OMG plc. Vicon Vero™ is a trademark of OMG plc. Other product and company names herein may be the trademarks of their respective owners.
Vicon Motion Systems is an OMG plc company.
Page 5
Regulatory information
Important
Radio and television interference
The following topics contain
information concerning compliance
with regulations of radio and television
interference:
❙ For United States of America
customers
❙ For Canadian customers
For United States of America
customers
Federal Communications Commission
(FCC) Part 15 Information
This equipment has been
tested and found to comply
with the limits for a Class A
digital device, pursuant to Part 15 of the
FCC Rules (CFR 47:Part 15:B:2013).
These limits are designed to provide
reasonable protection against harmful
interference when the equipment is
operated in a commercial environment.
This equipment generates, uses, and can
radiate radio frequency energy and, if
not installed and used in accordance
with the instruction manual, may cause
harmful interference to radio
communications. Operation of this
equipment in a residential area is likely
to cause harmful interference, in which
case the user will be required to correct
the interference at his own expense.
Properly shielded and grounded cables
and connectors must be used in order to
meet FCC emission limits. Vicon Motion
Systems Ltd is not responsible for any
radio or television interference caused
by using other than recommended
cables and connectors or by
unauthorized changes or modifications
to this equipment. Unauthorized
changes or modifications could void the
user's authority to operate the
equipment.
This device complies with Part 15 of the
FCC rules. Operation is subject to the
following two conditions: (1) this device
may not cause harmful interference, and
(2) this device must accept any
interference received, including
interference that may cause undesired
operation.
For Canadian customers
Conformity to the Canadian
Interference-Causing Equipment
Regulations
This Class A digital apparatus meets the
requirements of the Canadian
Interference-Causing Equipment
Regulations ICES-003:2004.
Avis de conformité à la réglementation
d'Industrie Canada
Cet appareil numérique de la classe A
respecte toutes les exigences du
Règlement sur le matériel brouilleur du
Canada ICES-003:2004.
Environmental regulations (European Union customers)
This section lists the directives that
apply to Vicon Vero systems.
This information applies only to
European Union member states.
Vicon meets these European
Commission directives concerning
waste electrical and electronic
equipment:
❙ Directives 2002/95/EC and 2011/65/
EU (for details, see Restriction of the
use of certain hazardous substances
in electrical and electronic
equipment – RoHS and recast (RoHS
2)).
❙ REACH Declaration of Conformity
❙ Directive 2202/96/EC (for details, see
Waste Electrical and Electronic
Equipment (WEEE)).
Restriction of the use of certain
hazardous substances in electrical and
electronic equipment – RoHS and recast
(RoHS 2)
This equipment is fully RoHS- and RoHS
2- compliant. RoHS Directive 2002/95/
EC provides that new electrical and
electronic equipment put on the market
for the first time from 1 July 2006 should
not contain lead, cadmium, mercury,
hexavalent chromium, polybrominated
biphenyls (PBB), or polybrominated
diphenyl ethers (PBDE). The European
Union Directive 2011/65/EU provides
that new electrical and electronic
equipment put on the market for the
first time from 3rd January 2014 shall
not contain more than permitted levels
of lead, cadmium, mercury, hexavalent
chromium, polybrominated biphenyls
(PBB), or polybrominated diphenyl
ethers (PBDE; PentaBDE, OctaBDE;
DecaBDE), Mercury (Hg).
REACH Declaration of Conformity
Vicon Motion Systems Ltd is a
manufacturer of electronic hardware.
We are therefore considered a
“downstream user” as far as the REACH
document is concerned. Vicon Motion
Systems Ltd is therefore not obligated to
register with the European Agency for
Chemicals ‘ECHA’.
Products sold by Vicon Motion Systems
Ltd are “articles” as defined in REACH
(Article 3 Definitions). Moreover and
under normal and reasonably
foreseeable circumstances of
application, the articles supplied shall
not release any substance. For that,
Vicon Motion Systems Ltd is neither
obligatory for registration nor for the
creation of material safety data sheets.
In order to assure our customers of the
continual supply of reliable and safe
products, we ensure that our suppliers
fulfill all requirements regarding
chemical substances and prepared
materials.
Vicon Vero Quick Start GuideMay 2016
Page 6
Regulatory information
Waste Electrical and Electronic Equipment (WEEE)
The use of the symbol as a marking on the equipment,
accessories or literature indicates that this product
and its electronic accessories (e.g. USB cable) may not
be treated as household waste. By ensuring this
product is disposed of correctly, you will help prevent
potential negative consequences for the environment and
human health, which could otherwise be caused by
inappropriate waste handling of this product.
Household users should contact either the retailer where they
purchased this device, or their local government office, for
details of where and how they can take these items for
environmentally safe recycling.
Business users should contact their supplier and check the
terms and conditions of the purchasing contract. This device
and its electronic accessories should not be mixed with other
commercial waste for disposal.
EU Declaration of Conformity (Vicon Vero cameras)
0088
Declaration of Conformity
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 14 Minns Estate
Oxford OX2 0JB
United Kingdom
declare that the VICON VERO 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 Vero cameras)
right, 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
20th April 2016
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 cameras)
This section 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 14 Minns Estate
Oxford OX2 0JB
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.
About your Vicon camera packaging
The box in which your new Vicon Vantage,
Vicon Vero or Vicon Vue camera arrived has a
specially formed foam insert that holds the
camera. This insert is made of a protective
material that prevents most damage that
could be caused during shipping. Vicon
recommends that you retain this box as it
provides the most convenient and safe way to
ship your camera(s) in future.
Vicon Vero Quick Start GuideMay 2016
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