Laerdal Nursing Anne Manual Del Usario página 58

한국어
Nursing Anne Simulator 규제 정보
USA and Canada
FCC
Federal Communications Commission
Statement and Industry Canada Statements
This device complies with part 15 of the FCC
rules and RSS-210 of the Industry Canada
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.
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.
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.
FCC ID 포함: QHQ-2011480
IC ID 포함: 20263-2011480
The term "IC" before the equipment certification
number only signifies that the Industry Canada
technical specifications were met.
Caution: Changes or modifications not
expressly approved by Laerdal Medical could
void the user's authority to operate the
equipment.
Le terme « IC » qui précède le numéro
d'agrément de l'équipement signifie uniquement
que les caractéristiques techniques spécifiées
par Industrie Canada sont respectées.
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.
방사선 노출 진술
이 장비는 관리되지 않은 환경에 대해 제시된
IC 방사선 노출 제한을 준수합니다. 이 장비는
라디에이터와 신체 사이 거리를 최소 20cm가
되도록 해 설치 및 작동해야 합니다.
EU
본 제품은 유무선 통신기기 지침(RED)
에 대해 Council Directive 2014/53/EU 및
특정유해물질 사용제한(RoHS)에 대해
Council Directive 2011/65/EU의 필수 요구
사항을 준수합니다.
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