NoRSK
INNHoLDSfoRTEGNELSE
1.1
1.2
Innføringssystem ................................................................................................. 88
1.3
2 TILTENKT BRUK ......................................................................................... 88
4.1
Generelt................................................................................................................... 88
4.2
4.3
4.4
Valg av anordning ............................................................................................... 88
4.5
4.6
4.7
MR-informasjon.................................................................................................... 89
6.1
8 LEVERINGSFORM ..................................................................................... 90
9.1
Legeopplæring ..................................................................................................... 90
Pasientutvalg ........................................................................................................ 90
9.2
Inspeksjon før bruk ............................................................................................. 90
9.3
Nødvendige materialer ..................................................................................... 90
9.4
Anbefalte materialer .......................................................................................... 90
9.5
implantatets diameter* .................................................................................... 91
implantatdiameter* ............................................................................................ 91
10 BRUKSANVISNING ................................................................................. 91
Anatomiske krav .................................................................................................. 91
Sluttangiogram .................................................................................................... 92
10.2 Hjelpeanordninger ............................................................................................. 92
Generell bruksinformasjon .............................................................................. 92
Sluttangiogram .................................................................................................... 93
OPPFØLGING .......................................................................................... 93
11.1 Generelt................................................................................................................... 93
11.4 MR-informasjon.................................................................................................... 94
I-ALPHA-TAA-1306-436-01
PoLSKI
SPIS TREŚCI
1 OPIS URZĄDZENIA ................................................................................... 95
1.1
1.2
System wprowadzający .................................................................................... 95
1.3
3 PRZECIWWSKAZANIA ............................................................................. 95
4.1
Ogólne ..................................................................................................................... 95
4.2
4.3
4.4
Wybór urządzenia ............................................................................................... 96
4.5
4.6
4.7
6.1
9.1
Szkolenie lekarza ................................................................................................. 97
Dobór pacjentów ................................................................................................ 97
9.2
Kontrola przed użyciem .................................................................................... 97
9.3
Wymagane materiały ......................................................................................... 97
9.4
Materiały zalecane .............................................................................................. 98
9.5
10 WSKAZÓWKI UŻYCIA ............................................................................ 99
Wymagania anatomiczne ................................................................................ 99
i dystalne................................................................................................................. 99
trzonu - opcjonalne ..........................................................................100
Angiogram końcowy .......................................................................................100
Angiogram końcowy .......................................................................................101
PO ZABIEGU .......................................................................................... 101
11.1 Ogólne ...................................................................................................................101
7