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Système Pour Genou BioniCare
®
FRANÇAIS
Recommandations et déclaration du fabricant - immunité électromagnétique
Test d’immunité Niveau de test CEI
60601
Niveau de
conformité
Environnement
électromagnétique -
recommandation
Surtension
CEI 61000-4-5
± 1 kV ligne(s)-
ligne(s)
± 2 kV ligne(s)-terre
Sans objet Sans objet
Chutes de tension,
brèves
< 5 % U
T
Sans objet Sans objet
Interruptions et
variations de tension
sur les lignes
d’alimentation
électrique
CEI 61000-4-11
(>95 % baisse in U
T
)
pour 0,5 cycle
40 % U
T
(60 % baisse in U
T
)
pour 5 cycles
70 % U
T
(30 % baisse in U
T
)
pour 25 cycles
< 5 % U
T
(>95 % baisse in U
T
)
pour 5 s
Champ magnétique
à la fréquence du
réseau (50/60 Hz)
CEI 61000-4-8
3 A/m Sans objet Sans objet
REMARQUE : U
T
est la tension secteur avant l’application du niveau de test .
Tableau de Conformité Électromagnétique (suite)
Conseils et déclaration du fabricant sur l’immunité électromagnétique
Le système pour genou BioniCare est destiné à un usage dans les environnements
électromagnétiques décrits ci-dessous. Le client ou l’utilisateur du système pour genou
BioniCare doit s’assurer que le système est utilisé dans un tel environnement.
Test
d’immunité
Niveau de
test CEI 60601
Niveau de
conformité
Environnement électromagnétique -
recommandation
Les appareils de communication RF portables
et mobiles ne doivent pas être utilisés à
une distance inférieure du système pour
genou BioniCare, à la distance de sécurité
recommandée calculée à partir de l’équation
applicable à la fréquence de l’émetteur.
94


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