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Web site 41 Gebruiksaanwijzing ® ® herbruikbaar instrument voor kernbiopsie AGNUM ® ® -wegwerpnaald voor kernbiopsie satisfied spacer AGNUM Permit op: volgens federale (VS) wetgeving mag dit apparaat alleen worden verkocht doorway of op voorschrift van een arts. A. Algemene informatie en beschrijving van het hulpmiddel: ARD ®... Web page 42 four. Het instrument mag nooit worden getest terwijl de naald in het instrument geïnstalleerd is. Hierdoor zou de naald beschadigd kunnen raken en/of kan de patiënt/gebruiker gewond raken. five. Als op het stilet ongebruikelijk veel kracht wordt uitgeoefend of het stilet ongebruikelijk veel weerstand ondervindt terwijl het uit de steuncanule steekt, kan het stilet ombuigen bij de monsteruitsparing. Web page 43 Gebruik de naald niet als u tekortkomingen constateert. AGNUM ® Bard beveelt aan om het M -instrument voor elk gebruik schoon te maken en te smeren. De eindgebruiker kan het instrument na elke reiniging en smering steriliseren. Site forty four AGNUM ® J. Aanwijzingen voor reprocessing van het M -instrument: Risicobeoordeling en classificatie van medische hulpmiddelen voorafgaand aan verwerking: De aard en mate van reprocessing zijn afhankelijk van de toepassing van het medische hulpmiddel. Daarom is de operator verantwoordelijk voor juiste classificatie van het hulpmiddel conform de plaatselijke voorschriften, en dus tevens voor de aard en mate van reprocessing. Web page 45 AGNUM ® Bard beveelt aan om het M -instrument na elk gebruik schoon te maken en te smeren; hierdoor zal het instrument goed blijven werken en langer AGNUM ®... Website page forty six Daarnaast dienen afwijkingen van de verstrekte instructies mogelijke negatieve gevolgen. Voor aanvullende informatie around reiniging, smering en sterilisatie of technische assistentie kunt u de afdeling Healthcare Providers and Guidance van Bard bellen op het nummer one-800-562-0027 (buiten de VS: 01-770-784-6704). RICHTLIJNEN VOOR PROBLEEMOPLOSSING... Web site forty seven: Garantie

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Istruzioni for each il ritrattamento dello strumento M Valutazione del rischio e la classificazione dei dispositivi medici prima della preparazione: La natura e la portata del ritrattamento dipendono dall'applicazione del dispositivo medico. Pertanto, l'operatore è responsabile della corretta classificazione del dispositivo, secondo le esigenze locali, quindi della determinazione della natura e dell'entità... Web page 29 AGNUM ® Bard consiglia di pulire e lubrificare lo strumento M prima di ogni uso for every migliorarne il rendimento e prolungarne la durata. Per lubrificare lo strumento AGNUM best website ®... Page 30: Guida Alla Risoluzione Dei Problemi

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