ActiGraph LEAP Instructions For Use Manual page 14

Regulatory Information
Emergo Europe
Westervoortsedijk 60
6827 AT Arnhem
The Netherlands
AUSTRALIAN SPONSOR
Emergo Australia
Level 20, Tower II
Darling Park
201 Sussex Street
Sydney NSW 2000
Australia
Emergo Consulting (UK)
Limited
c/o Cr360 – UL
International
Compass House, Vision
Park Histon
Cambridge CB24 9BZ
United Kingdom
21490-23-09607
"Este equipamento não tem direito à
proteção contra interferência prejudicial e
não pode causar interferência em sistemas
devidamente autorizados."
Para maiores informações, consulte o site
da ANATEL – www.anatel.gov.br
STM2XXXXXXXXX
MODEL: LEAP | E.200.6025 | RELEASED: 07/12/2024 | REV: 2
Authorized Representative in European Community
Indicates the authorized representative in the European Community.
ActiGraph's Australia Sponsor
Indicates ActiGraph's authorized Australian Sponsor.
ActiGraph's United Kingdom Sponsor
Indicates ActiGraph's authorized United Kingdom Sponsor.
Catalog Number
Indicates the manufacturer's catalogue number so that the medical device can
be identified for reordering.
CE Symbol
By affixing 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.
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 specific medical device can
be identified. The manufacturing date is included in the serial number.
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