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Hinweise und Herstellererklärung
Elektromagnetische Emissionen Hinweise und Herstellererklärung
Die MiniMed 640G Insulinpumpe ist für die Nutzung in dem nachfolgend spezifizier‐
ten elektromagnetischen Umfeld vorgesehen. Der Käufer oder Anwender der
MiniMed Insulinpumpe sollte sicherstellen, dass diese in einem solchen Umfeld ver‐
wendet wird.
Emissionstest Einhaltung Elektromagnetisches Umfeld Hin‐
weise
HF-Emissionen
Test: 47 CFR
Abschnitt 15, Unter‐
abschnitt C Kapi‐
tel 15.247(a)(2)/
RSS-210 FHSS–
DAOO-705, DTS-KDB
558074, ANSI C63.4,
RSS-Gen, FCC
Abschnitt 15 Kapi‐
tel 15.109, Klasse B/
ANSI c63.4 (2009)
6-dB- und 99-%-
Bandbreiten: Bestan‐
den
Maximale Ausgangs‐
leistung: Bestanden
Störende ausgesen‐
dete Emissionen:
Bestanden
Leistungsspektral‐
dichte: Bestanden
Die MiniMed Insulinpumpe muss elekt‐
romagnetische Energie aussenden, um
ihre bestimmungsgemäße Funktion zu
erfüllen. Benachbarte elektronische
Geräte können davon beeinträchtigt
werden.
HF-Emissionen
EN55011 (2009)+A1
Klasse B Die MiniMed Insulinpumpe kann in
Flugzeugen und sämtlichen Einrichtun‐
gen verwendet werden, einschließlich
häuslicher Einrichtungen und Einrich‐
tungen, die direkt an das öffentliche
Niederspannungs-Stromversorgungs‐
netz zur Versorgung von Wohngebäu‐
den angeschlossen sind.
RTCA DO 160G
(2010) 20.5 und 21.5
Konform
ARIB STD-T66 Konform
produktspezifikationen und sicherheitsinformationen
Produktspezifikationen und Sicherheitsinformationen 311
Version: 06-20-2017 PatchIFU_PrinterMarks.xsl Language: de
325


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Medtronic MiniMed 640G User Manual - Dutch - 331 pages


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