15
Federal Communications Commission
(FCC) and Industry Canada (IC) Statements
This device complies with part 15 of the FCC
Rules and RSS-210 of IC 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.
This equipment has been tested and found
to comply with the limits for a Class B digital
device, pursuant to part 15 of the FCC
Rules. These limits are designed to provide
reasonable protection against harmful
interference in a residential installation. This
equipment generates, uses and can radiate
radio frequency energy and, if not installed
and used in accordance with the instructions,
may cause harmful interference to radio
communications. However, there is no
guarantee that interference will not occur
in a particular installation. If this equipment
does cause harmful interference to radio or
television reception, which can be determined
by turning the equipment off and on, the
user is encouraged to try to correct the
interference by one or more of the following
measures:
• Reorient or relocate the receiving antenna.
• Increase the separation between the
equipment and receiver.
• Consult the dealer or an experienced
radio/TV technician for help.
Caution: Changes or modifications not
expressly approved by Laerdal Medical could
void the user’s authority to operate the
equipment.
The term “IC” before the equipment
certification number only signifies that the
Industry Canada technical specifications
were met.
Mise en garde: Tout changement ou toute
modification n’ayant pas fait l’objet d’une
approbation expresse de Laerdal Medical peut
annuler le droit dont dispose l’utilisateur de se
servir de l’équipement.
Le terme « IC » qui précède le numéro
d’agrément de l’équipement signifie
uniquement que les caractéristiques
techniques spécifiées par Industrie Canada
sont respectées.
This device contains licence-exempt
transmitter(s)/receiver(s) that comply with
Innovation, Science and Economic Development
Canada’s licence-exempt RSS(s). Operation is
subject to the following two conditions:
1.
This device may not cause interference.
2.
This device must accept any interference,
including interference that may cause
undesired operation of the device.
L’émetteur/récepteur exempt de licence contenu
dans le présent appareil est conforme aux
CNR d’Innovation, Sciences et Développement
économique Canada applicables aux appareils
radio exempts de licence. L’exploitation est
autorisée aux deux conditions suivantes :
1.
L’appareil ne doit pas produire de
brouillage;
2.
L’appareil doit accepter tout brouillage
radioélectrique subi, même si le
brouillage est susceptible d’en
compromettre le fonctionnement.
FCC-ID: QHQ-212-00001 (SimMan 3G only)
Canada
Canadian ICES-003 Statement
This Class B digital apparatus complies with
Canadian ICES-003.
Cet appareil numérique de la classe B est
conforme à la norme NMB-003 du Canada.
EU
Dieses Produkt entspricht den grundlegenden
Anforderungen der Richtlinie des Rates
2014/53/EU über Funkanlagen (RED) sowie
der Richtlinie des Rates 2011/65/EU zur
Beschränkung der Verwendung bestimmter
gefährlicher Stoffe in Elektro- und
Elektronikgeräten (RoHS).
Deutsch
SimMan
Gesetzliche Anforderungen
Summary of Contents for SimMan
Page 1: ...EN www laerdal com IT BR NL JA ZH FR DE ES KO PL SimMan Important Product Information...
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Page 43: ...43 SimMan SimMan Laerdal Medical SimMan 2015 CPR SimMan ECG...
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Page 46: ...46 SimMan CE WEEE 2012 19 EC Laerdal SimMan Laerdal www laerdal com jp...
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Page 51: ...51 SimMan CE 2012 19 EC WEEE SimMan Li Ion www laerdal com cn...
Page 53: ...53 SimMan SimMan Patient Simulator Laerdal Medical SimMan CPR 2015 SimMan ECG ECG ECG...
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Page 56: ...56 SimMan CE WEEE 2012 19 EC Laerdal SimMan Li Ion Laerdal http www laerdal com kr...
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