Table Of Contents - Abilia Control Omni Converter Installation Manual

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Contents
Beskrivning .............................................................................................. 4
Inkoppling ................................................................................................ 4
Viktigt ...................................................................................................... 5
Byte av säkring ........................................................................................ 5
Tekniska Data ......................................................................................... 5
Överensstämmelse med Medicintekniska direktivet ................................ 5
Description .............................................................................................. 6
Wiring ...................................................................................................... 6
Important ................................................................................................. 7
Fuse Replacement .................................................................................. 7
Technical Data ........................................................................................ 7
Compliance with the Medical Device Directive ........................................ 7
Description .............................................................................................. 8
Câblage ................................................................................................... 8
Important ................................................................................................. 9
Changement de fusible ........................................................................... 9
Caractéristiques techniques .................................................................... 9
Directive sur les dispositifs médicaux ...................................................... 9
DE: Montageanleitung für Control Omni Converter .................................. 10
Beschreibung ........................................................................................ 10
Anschließen .......................................................................................... 10
Wichtig .................................................................................................. 11
Austausch der Sicherung ...................................................................... 11
Technische Daten ................................................................................. 11
Konformität mit Medizinprodukte-Richtlinie: ........................................... 11
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