Arthrex AR-3210-0006 Instrucciones De Uso página 207

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1
Viktiga anvisningar............................................................................................................................................................. 3
2
Säkerhetsanvisningar ......................................................................................................................................................... 4
3
Allmän information ............................................................................................................................................................ 5
3.1
Beskrivning av apparaten ...................................................................................................................................................... 5
3.1.1
Välja brännvidd ......................................................................................................................................................................... 5
3.1.2
Välja fokusområde ................................................................................................................................................................... 6
3.2
Avsedd användning ................................................................................................................................................................. 6
3.3
Kontraindikationer................................................................................................................................................................... 6
3.4
Allmänna varningar och försiktighetsåtgärder............................................................................................................... 7
3.4.1
Allmänna varningar................................................................................................................................................................. 7
3.4.2
Försiktighetsåtgärder.............................................................................................................................................................. 8
4
Idrifttagning........................................................................................................................................................................ 9
4.1
Ansluta videoobjektivet till en C-Mount-kamera............................................................................................................ 9
4.2
Ansluta videoobjektivet till endoskopet............................................................................................................................ 9
4.3
Använda sterilt överdrag........................................................................................................................................................ 9
5
Visuell inspektion och funktionskontroll ........................................................................................................................... 11
5.1
Visuell inspektion ..................................................................................................................................................................... 11
5.2
Funktionskontroll ..................................................................................................................................................................... 11
6
Rekonditionering och underhåll......................................................................................................................................... 13
6.1
Förbereda rekonditioneringen ............................................................................................................................................. 13
6.2
Maskinell rengöring................................................................................................................................................................. 13
6.2.1
Maskinell desinfektion............................................................................................................................................................ 14
6.2.2
Maskinell torkning ................................................................................................................................................................... 14
6.3
Manuell rengöring ................................................................................................................................................................... 15
6.3.1
Manuell desinfektion .............................................................................................................................................................. 15
6.3.2
Manuell torkning...................................................................................................................................................................... 15
6.4
Validering av rekonditioneringen ........................................................................................................................................ 16
6.4.1
Manuell rekonditionering...................................................................................................................................................... 16
6.4.2
Maskinell rekonditionering ................................................................................................................................................... 16
7
Sterilisering ......................................................................................................................................................................... 17
7.1
Förpackning ............................................................................................................................................................................... 17
7.2
Sterilisering med fuktig värme............................................................................................................................................. 17
7.3
Lågtemperatursterilisering.................................................................................................................................................... 18
7.4
Förvaring..................................................................................................................................................................................... 18
7.5
Validering av steriliseringen.................................................................................................................................................. 18
8
Tekniska data ...................................................................................................................................................................... 19
9
Serviceadresser och reparationer ....................................................................................................................................... 20
Index.................................................................................................................................................................................... 21
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