4
5
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.
Resusci Baby QCPR Contains
FCC ID: QHQ 20-10494
IC 20263-2010494
Canada
This Class B digital apparatus complies with
Canadian ICES-003.
English
Resusci Baby
QCPR / QCPR with Airway Head
Содержание Resusci Baby QCPR
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