Inhoudsopgave
Advertenties
SVENSKA
Inhoudsopgave
...........................................................................................................................................4
◦
1.1 Opmerkingen over deze gebruiksaanwijzing .................................................................................4
◦
1.2 Omgevingscondities.......................................................................................................................4
◦
1.3 Verzending en uitpakken ...............................................................................................................4
◦
1.4 Waarschuwingen m.b.t. installatie .................................................................................................5
◦
1.5 Bediening, omgeving .....................................................................................................................5
◦
1.6 Lichttoxiciteit ..................................................................................................................................5
◦
1.7 Desinfectie .....................................................................................................................................6
◦
1.8 Garantie en productaansprakelijkheid ...........................................................................................6
◦
1.9 Rapportageverplichting ..................................................................................................................6
◦
1.10 Symboolbeschrijving ....................................................................................................................6
............................................................................................6
◦
2.1 Beschrijving van het apparaat........................................................................................................6
▪
2.1.1 Beoogde gebruikers............................................................................................................7
◦
2.2 Medisch doel..................................................................................................................................7
▪
2.2.1 Indicaties.............................................................................................................................7
▪
2.2.2 Deel van het lichaam ..........................................................................................................7
▪
2.2.3 Patiëntenpopulatie ..............................................................................................................7
▪
2.2.4 Contra-indicaties.................................................................................................................7
◦
2.3 Werkingsprincipes..........................................................................................................................7
▪
2.3.1 Bedieningsomgeving ..........................................................................................................7
◦
2.4 Klinisch voordeel............................................................................................................................8
..............................................................................................................................................8
◦
3.1 Overzicht........................................................................................................................................8
◦
4.1 Microscoop en belichting ...............................................................................................................9
◦
4.2 Voedingsadapter............................................................................................................................9
◦
4.3 Instrumentenbasis met gewichtscompensatie ...............................................................................9
◦
4.4 Gewichtscompensatie instellen......................................................................................................9
◦
4.5 Gewichtscompensatie inschakelen................................................................................................9
◦
4.6 Gewichtscompensatie uitschakelen.............................................................................................10
◦
4.7 De beweeglijkheid van de spleetinstelling regelen ......................................................................10
...........................................................................................................................10
◦
5.1 Apparaat inschakelen ..................................................................................................................10
........................................................................................................................................10
◦
6.1 Oculairs instellen..........................................................................................................................10
◦
6.2 Patiënten voorbereiden................................................................................................................11
◦
6.3 Bediening van het apparaat .........................................................................................................11
◦
6.4 Filters en diafragma's instellen.....................................................................................................12
◦
6.5 Fixatiester ....................................................................................................................................12
◦
6.6 Microscoop en oculair ..................................................................................................................13
© HAAG-STREIT AG, 3098 Koeniz, Switzerland - HS-Doc. no. 1500.7220589-04210 - 2021 - 08
NEDERLANDS
PORTUGUÊS
...............................................................................9
ESPAÑOL
ITALIANO
............................................................................................................... 13
............................................................................................................. 13
◦
8.1 Spleetbelichting ........................................................................................................................... 13
◦
8.2 Stereomicroscoop........................................................................................................................ 14
◦
8.3 Instrumentenbasis ....................................................................................................................... 14
◦
8.4 Afmetingen .................................................................................................................................. 14
..................................................................................................................................... 14
◦
9.1 Apparaatcontrole ......................................................................................................................... 14
◦
9.2 Service en onderhoud ................................................................................................................. 14
◦
9.3 Reiniging en desinfectie .............................................................................................................. 14
◦
9.4 De belichtingsspiegel vervangen................................................................................................. 15
◦
9.5 Stofkap ........................................................................................................................................ 15
............................................................................................................................................ 15
◦
10.1 Accessoires / functionele onderdelen / afneembare onderdelen / verbruiksartikelen ............... 15
◦
10.2 Wettelijke voorschriften ............................................................................................................. 16
◦
10.3 Classificering ............................................................................................................................. 16
◦
10.4 Verwijdering............................................................................................................................... 16
◦
10.5 Geldende normen...................................................................................................................... 16
◦
compatibiliteit (EMC) ......................................................................................................................... 17
▪
10.6.1 Algemeen ....................................................................................................................... 17
▪
10.6.2 Storingsemissie .............................................................................................................. 17
▪
10.6.3 Op elektromagnetische immuniteit geteste omgeving (deel 1) ...................................... 18
▪
10.6.4 Op elektromagnetische immuniteit geteste omgeving (deel 2) ...................................... 19
▪
10.6.5 Aanbevolen scheidingsafstanden tussen draagbare en mobiele RF-
communicatieapparatuur en dit product .................................................................................... 21
FRANÇAIS
DEUTSCH
ENGLISH
3
Advertenties
Inhoudsopgave
