Inhoudsopgave
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SVENSKA
Inhoudsopgave
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1.1 Opmerkingen over deze gebruiksaanwijzing .................................................................................4
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1.2 Omgevingscondities.......................................................................................................................4
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1.3 Verzending en uitpakken ...............................................................................................................4
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1.4 Waarschuwingen m.b.t. installatie .................................................................................................4
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1.5 Bediening, omgeving .....................................................................................................................5
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1.6 Desinfectie .....................................................................................................................................6
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1.7 Garantie en productaansprakelijkheid ...........................................................................................6
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1.8 Rapportageverplichting ..................................................................................................................6
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1.9 Symboolbeschrijving ......................................................................................................................6
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2.1 Beschrijving van het apparaat........................................................................................................6
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2.1.1 Beoogde gebruikers............................................................................................................7
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2.2 Medisch doel..................................................................................................................................7
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2.2.1 Indicaties.............................................................................................................................7
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2.2.2 Deel van het lichaam ..........................................................................................................7
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2.2.3 Patiëntenpopulatie ..............................................................................................................7
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2.2.3.1 Contra-indicaties......................................................................................................7
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2.3 Werkingsprincipes..........................................................................................................................7
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2.3.1 Bedieningsomgeving ..........................................................................................................7
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2.4 Klinisch voordeel............................................................................................................................7
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3.1 Beschrijving van het apparaat........................................................................................................8
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3.2 Systeemcomponenten ...................................................................................................................8
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3.3 Overzicht van apparaat..................................................................................................................8
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3.4 Lcd-display.....................................................................................................................................9
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3.5 Bedieningspaneel ..........................................................................................................................9
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3.6 Aansluitingen .................................................................................................................................9
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3.7 Behuizing .......................................................................................................................................9
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3.8 Koepel..........................................................................................................................................10
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3.9 Voorhoofdsteun............................................................................................................................10
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3.10 Kinsteun .....................................................................................................................................10
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3.11 Zwenkeenheid............................................................................................................................10
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3.12 Correctieglashouder...................................................................................................................10
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3.13 Patiëntantwoordknop .................................................................................................................10
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3.14 Netwerkaansluiting.....................................................................................................................10
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3.15 Lichtbronnen ..............................................................................................................................10
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3.16 Lichtsterkten...............................................................................................................................10
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3.17 Prikkel ........................................................................................................................................11
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3.18 Omgevingsbelichting..................................................................................................................11
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3.19 Fixatiemarkering ........................................................................................................................11
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3.20 Fixatiecontrole............................................................................................................................11
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3.21 Onderzoeksgegevens ................................................................................................................11
© HAAG-STREIT AG, 3098 Koeniz, Switzerland - HS-Doc. no. 1500.7220343-04110 - 2022 - 10
NEDERLANDS
PORTUGUÊS
ESPAÑOL
ITALIANO
FRANÇAIS
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4.1 Transport van het apparaat ......................................................................................................... 11
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4.2 Patiëntantwoordknop aansluiten ................................................................................................. 12
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4.3 Netwerkkabel aansluiten ............................................................................................................. 12
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4.4 Netstroomkabel aansluiten .......................................................................................................... 12
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6.1 Apparaat inschakelen .................................................................................................................. 14
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6.2 Apparaat uitschakelen ................................................................................................................. 14
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7.1 Aanpassen aan de patiënt........................................................................................................... 14
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9.1 Octopus 900 ................................................................................................................................ 14
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9.2 IR-belichting................................................................................................................................. 15
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9.3 Gezichtsveld ................................................................................................................................ 15
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9.4 Octopus 900-besturing/pc ........................................................................................................... 15
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10.1 Service en onderhoud ............................................................................................................... 15
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10.2 Reiniging en desinfectie ............................................................................................................ 15
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10.2.1 Apparaat in het algemeen .............................................................................................. 16
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10.2.2 Display, bedieningspaneel ............................................................................................. 16
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10.2.3 Koepel ............................................................................................................................ 16
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10.2.4 Toepassingsgedeelten ................................................................................................... 16
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10.2.5 Hulpmiddelen ................................................................................................................. 16
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10.3 Lichtbronnen.............................................................................................................................. 16
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10.4 Stofkap ...................................................................................................................................... 16
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11.1 Accessoires / verbruiksmaterialen / reserveonderdelen / upgrades.......................................... 17
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11.2 Wettelijke voorschriften ............................................................................................................. 17
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11.3 Classificering ............................................................................................................................. 17
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11.4 Verwijdering............................................................................................................................... 17
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11.5 Geldende normen...................................................................................................................... 17
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11.6 EMC-supplement....................................................................................................................... 18
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11.6.1 Algemeen ....................................................................................................................... 18
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11.6.2 Storingsemissie .............................................................................................................. 19
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11.6.3 Op elektromagnetische immuniteit geteste omgeving (deel 1) ...................................... 20
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11.6.4 Op elektromagnetische immuniteit geteste omgeving (deel 2) ...................................... 21
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DEUTSCH
ENGLISH
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