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........................................................................................................7
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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............................................................................................................................8
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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 Gebruikersinterface (14) ................................................................................................................9
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3.5 Behuizing .......................................................................................................................................9
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3.6 Voorhoofdsteun..............................................................................................................................9
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3.7 Kinsteun (optioneel) .......................................................................................................................9
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3.8 Nabijcorrectielens ..........................................................................................................................9
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3.9 Afdekking patiëntzijde ....................................................................................................................9
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3.10 Correctieglazen..........................................................................................................................10
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3.11 Aansluitingen .............................................................................................................................10
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3.11.1 USB-aansluitingen ..........................................................................................................10
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3.11.2 Aansluiting op het elektriciteitsnet ..................................................................................10
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3.11.3 Ethernetaansluiting .........................................................................................................10
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3.12 Led-achtergrondverlichting ........................................................................................................10
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3.13 Fixatiecontrole............................................................................................................................10
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3.14 Onderzoeksgegevens ................................................................................................................10
¥ 4 Montage/installatie van het apparaat
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4.1 Transport van het apparaat..........................................................................................................11
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4.2 Patiëntantwoordknop aansluiten..................................................................................................11
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4.3 Stroomkabel aansluiten ...............................................................................................................11
© HAAG-STREIT AG, 3098 Koeniz, Switzerland - HS-Doc. no. 1500.7220367-04110 - 2022 - 10
NEDERLANDS
PORTUGUÊS
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ESPAÑOL
ITALIANO
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5.1 Systeemvarianten, Octopus 600 met printer ............................................................................... 12
.......................................................................................................................... 13
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6.1 Apparaat inschakelen .................................................................................................................. 13
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6.2 Apparaat uitschakelen ................................................................................................................. 13
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7.1 Aanpassen aan de patiënt........................................................................................................... 13
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9.1 Octopus 600 ................................................................................................................................ 13
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9.2 IR-belichting................................................................................................................................. 14
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9.3 Afmetingen .................................................................................................................................. 14
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9.4 Gezichtsveld ................................................................................................................................ 14
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10.1 Service en onderhoud ............................................................................................................... 14
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10.2 Reiniging en desinfectie ............................................................................................................ 14
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10.2.1 Apparaat in het algemeen .............................................................................................. 15
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10.2.2 Aanraakscherm .............................................................................................................. 15
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10.2.3 Toepassingsgedeelten ................................................................................................... 15
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10.2.4 Hulpmiddelen ................................................................................................................. 15
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10.3 Stofkap ...................................................................................................................................... 15
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11.1 Accessoires / verbruiksmaterialen / reserveonderdelen / upgrades.......................................... 15
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11.2 Wettelijke voorschriften ............................................................................................................. 16
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11.3 Classificering ............................................................................................................................. 16
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11.4 Verwijdering............................................................................................................................... 16
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11.5 Geldende normen...................................................................................................................... 16
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11.6 EMC-supplement....................................................................................................................... 16
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11.6.1 Algemeen ....................................................................................................................... 16
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11.6.2 Storingsemissie .............................................................................................................. 17
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11.6.3 Op elektromagnetische immuniteit geteste omgeving (deel 1) ...................................... 18
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11.6.4 Op elektromagnetische immuniteit geteste omgeving (deel 2) ...................................... 19
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FRANÇAIS
DEUTSCH
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ENGLISH
3
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Inhoudsopgave
