99
Federal Communications
Commission Statement
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.
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.
• Connect the equipment into an outlet
on a circuit different from that to which
the receiver is connected.
• 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.
Industry Canada Statement
This device complies with RSS-210 of
the Industry Canada Rules. Operation is
subject to the following two conditions:
1.This device may not cause harmful
interference.
2.This device must accept any interference
received, including interference that may
cause undesired operation.
Caution: Changes or modifications not
expressly approved by Laerdal Medical
could void the user’s authority to operate
the equipment.
Ce dispositif est conforme à la norme
CNR-210 d’Industrie Canada applicable
aux appareils radio exempts de licence.
Son fonctionnement est sujet aux deux
conditions suivantes:
1. le dispositif ne doit pas produire de
brouillage préjudiciable, et
2. ce dispositif doit accepter tout
brouillage reçu, y compris un
brouillage susceptible de provoquer un
fonctionnement indésirable.
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.
The term “IC” before the equipment
certification number only signifies that the
Industry Canada technical specifications
were met.
Le terme « IC » qui précède le numéro
d’agrément de l’équipement signifie
uniquement que les caractéristiques
techniques spécifiées par Industrie Canada
sont respectées.
Français
Informations réglementaires afférentes à Laerdal-SonoSim
