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1.
INLEIDING .............................................................................................................................................. 8
Indicaties ......................................................................................................................................... 10
Beoogde gebruikers ............................................................................................................ 10
Beoogde gebruiksomgeving ................................................................................................ 10
Contra-indicatiess ........................................................................................................................... 10
Veiligheid......................................................................................................................................... 10
Waarschuwingen................................................................................................................. 10
Let op .................................................................................................................................. 11
Voorzorgsmaatregelen ........................................................................................................ 12
Opmerkingen ...................................................................................................................... 12
Bewaren en hantering..................................................................................................................... 13
Symbolen ........................................................................................................................................ 14
Cyberveiligheid ................................................................................................................................ 15
2
CONFORMITEIT MET WET- EN REGELGEVING .................................................................................... 17
Conformiteit met normen en richtlijnen ........................................................................................ 17
RF-conformiteit ............................................................................................................................... 22
Verenigde Staten ................................................................................................................. 22
Canada ................................................................................................................................ 22
Japan ................................................................................................................................... 22
Essentiële prestaties ....................................................................................................................... 22
Afwijking van de normen ................................................................................................................ 23
3
OVERZICHT VAN HET OPTOMONITOR 3-SYSTEEM ............................................................................. 24
Optische module OptoMonitor 3 (OpM3-OU) ................................................................................ 26
Interfacekabels katheterisatiekamer .............................................................................................. 27
AUX In (AUX-interfacekabel) ............................................................................................... 27
Aortic In (interfacekabel aortadruk-omvormer, AO) .......................................................... 27
Aortic Out (drukuitgangsinterfacekabel) ............................................................................ 27
Distal Out (drukuitgangsinterfacekabel) ............................................................................. 27
Weergavescherm OptoMonitor 3 (OpM3-DU) ............................................................................... 27
Overzicht van het weergavescherm (DU) ........................................................................... 28
Koppelingseenheid OptoMonitor 3 (OpM3-HU)............................................................................. 29
Accessoires ...................................................................................................................................... 29
Drukgevoelige OptoWire-geleidingsdraad (niet meegeleverd) .......................................... 29
Aortadruk-omvormer (wordt door derden geleverd) ......................................................... 29
Geluidssignalen en led-indicatoren ................................................................................................ 30
Geluidssignalen ................................................................................................................... 30
Led-indicatoren ................................................................................................................... 31
Grafische gebruikersinterface ......................................................................................................... 33
Schermfuncties hoofdmenu ............................................................................................................ 35
LBL-2008-41-v5 OptoMonitor 3 Gebruiksaanwijzing_nl versie 2021-08
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