Hillrom Ultrafins Stirrups O-UFAS Instrucciones De Uso página 82

BRUGSANVISNING
Indholdsfortegnelse
Ultrafins® Stirrups (O-UFAS)
1 Generelle oplysninger: ...................................................................................................... 84
1.1 Ophavsret: .................................................................................................................. 84
1.2 Varemærker: .............................................................................................................. 84
1.3 Kontaktoplysninger: ................................................................................................... 85
1.4 Sikkerhedsovervejelser: .............................................................................................. 85
1.4.1 Meddelelse om sikkerhedssymbol for fare: .................................................. 85
1.4.2 Meddelelse om misbrug af udstyret: ............................................................ 85
1.4.3 Meddelelse til brugere og/eller patienter: ................................................... 85
1.4.4 Sikker bortskaffelse:.......................................................................................... 86
1.5 Betjening af systemet: ............................................................................................... 86
1.5.1 Relevante symboler: ....................................................................................... 86
1.5.2 Tilsigtet bruger og patientpopulation: .......................................................... 87
1.5.3 Overholdelse af lovgivning om medicinsk udstyr: ...................................... 88
1.6 Overvejelser vedr. elektromagnetisk kompatibilitet (EMC): ................................ 88
1.7 Autoriseret repræsentant i EU: ................................................................................. 88
1.8 Produktionsoplysninger:............................................................................................. 88
1.9 Oplysninger om EU-importør: .................................................................................... 88
1.10 Oplysninger om australsk sponsor: ........................................................................... 88
2 System ................................................................................................................................. 89
2.1 Identifikation af systemkomponenter: .................................................................... 89
2.2 Produktkode og beskrivelse:..................................................................................... 89
2.3 Tabel over tilbehør og forbrugsmaterialer: ............................................................. 90
2.4 Kliniske fordele: ........................................................................................................... 90
2.4.1 Indikationer for anvendelse: .......................................................................... 90
2.4.2 Tilsigtet anvendelse: ........................................................................................ 91
2.5 Restrisiko: ..................................................................................................................... 91
3 Opsætning og brug af udstyret: ..................................................................................... 91
3.1 Før brug: ...................................................................................................................... 91
3.2 Opsætning: ................................................................................................................. 91
3.3 Enhedens betjeningsknapper og indikatorer: ....................................................... 94
Document Number: 80028130
Version: B
Side 82
Issue Date: 06 MAR 2020
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