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INHOUDSOPGAVE
Hoofdstuk 1: INTRODUCTIE .................................................................................................................... 5
Hoofdstuk 2: SYMBOOL EN INDICATIES ................................................................................................. 6
2.1 SYMBOOL EN BESCHRIJVING ........................................................................................................ 6
2.2 WAARSCHUWINGEN ..................................................................................................................... 7
2.2.1 ALGEMENE WAARSCHUWINGEN ........................................................................................... 7
2.2.2 ELEKTRISCHE GEVAREN .......................................................................................................... 8
2.2.3 ELEKTROMAGNETISCHE VERSTORINGEN EN ELEKTROSTATISCHE ONTLADING .................... 9
2.2.4 OMGEVING ............................................................................................................................. 9
2.3 STORINGEN ................................................................................................................................. 10
Hoofdstuk 3: PRODUCTOMSCHRIJVING ............................................................................................... 11
3.1 ALGEMENE BESCHRIJVING ......................................................................................................... 11
3.2 BEOOGD GEBRUIK....................................................................................................................... 12
3.3 CONTRA-INDICATIES ................................................................................................................... 12
3.4 PRESTATIE EN VEILIGHEID .......................................................................................................... 12
3.5 CONFORM GEBRUIK ................................................................................................................... 13
3.6 ONDERDELENLIJST ...................................................................................................................... 14
3.7 COMPATIBILITEITEN ................................................................................................................... 15
Hoofdstuk 4: SYSTEEMCONFIGURATIE ................................................................................................ 17
4.1 INSTALLATIE VAN DE APPARATUUR .......................................................................................... 17
4.2 CONFIGURATIE EP-OPNAMESYSTEEM ....................................................................................... 19
4.2.1 CONFIGURATIE MET GE CARDIOLAB™ ................................................................................. 19
4.2.2 CONFIGURATIE MET BOSTON SCIENTIFIC LAB SYSTEM™ PRO ............................................. 21
4.2.3 CONFIGURATIE KARTERINGSKATHETER ............................................................................... 22
Hoofdstuk 5: CONFIGURATIE APPARATUUR ........................................................................................ 23
5.1 INSTELLINGEN ............................................................................................................................. 23
5.1.1 KATHETERSELECTIE ............................................................................................................... 23
5.1.2 INSTELLEN VERSTERKINGSWAARDEN .................................................................................. 23
5.1.3 SELECTIE STABIELE MODUS .................................................................................................. 24
5.2 PROCEDURE-INFORMATIE .......................................................................................................... 25
5.3 SMS VERIFICATIEPROCEDURE .................................................................................................... 26
5.4 VALIDATIE ELEKTROGRAMMEN ................................................................................................. 27
5.5 GEBRUIKERSINTERFACE .............................................................................................................. 28
5.6 BEKIJKEN PATIËNTENONDERZOEK ............................................................................................. 29
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P.N.: I001-1.4
Februari 2023
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