ActiGraph CPW01 - Page 26

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THEACTIGRAPH.COM
CENTREPOINT INSIGHT WATCH | E.200.6002 | RELEASED: 01/09/2023 | REV: 7
Regulatory Information | Continued
Authorized Representative in European Community
Indicates the authorized representative in the European Community.
ActiGraph’s Australia Sponsor
Indicates ActiGraph’s authorized Australian Sponsor.
Catalog Number
Indicates the manufacturer’s catalogue number so that the medical device can be
identied for reordering.
CE Symbol
By axing the CE marking to a product, a manufacturer declares that the product
meets all the legal requirements for CE marking and can be sold throughout the
EEA. ActiGraph’s products abide with the Medical Device Directive 93/42/EEC and
Radio Equipment Directive 2014/53/EU.
Brazil National Telecommunications Agency (ANATEL)
Homologação Number
This equipment operates on a secondary basis, that is, not entitled to protection
from harmful interference, even for stations of the same type, and may not cause
interference to systems operating on a primary basis.
Consult Instructions for Use
Indicates the need for the user to consult the instructions for use.
Serial Number
Indicates the manufacturer’s serial number so that a specic medical device can
be identied.
Emergo Europe
Prinsessegracht 20
2514 AP The Hague
The Netherlands
AUSTRALIAN SPONSOR
Emergo Australia
Level 20, Tower II
Darling Park
201 Sussex Street
Sydney NSW 2000
Australia
“Este equipamento não tem direito à
proteção contra interferência prejudicial e
não pode causar interferência em sistemas
devidamente autorizados.”
06584-19-09607
10 ISO 3864-1