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Sočasni razvoj medicinskega sterilizatorja z njegovo IEC 61010 verifikacijo
ID Turk, Andraž (Author), ID Jenko, Marjan (Mentor) More about this mentor... This link opens in a new window

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Abstract
Diplomska naloga obravnava sočasen razvoj medicinskega sterilizatorja za endoskope in doseganje skladnosti s standardom IEC 61010. Namesto tradicionalnega sekvenčnega razvoja smo uporabili sočasni pristop za optimizacijo regulacije temperature. Razvili smo regulator, programsko kodo, električno shemo in vezje za natančno upravljanje temperature komore. Testiranje je potrdilo skladnost sterilizatorja s standardom ISO 15883. Opravili smo varnostne preizkuse po standardu IEC 61010. Z zgodnjo vključitvijo verifikacije smo skrajšali razvojni čas in optimirali stroške izdelave sterilizatorja. Sočasen razvoj je omogočil hkratno validacijo programske in strojne opreme, kar rezultira tudi v zanesljivosti delovanja in holistični skladnosti naprave. Rezultati potrjujejo, da sočasno preverjanje skladnosti med razvojem bistveno pospeši certificiranje, hkrati pa zagotavlja visok nivo varnosti in zanesljivosti naprave.

Language:Slovenian
Keywords:skladnost naprav, IEC 61010, meritve, sočasni razvoj, sterilizatorji
Work type:Bachelor thesis/paper
Typology:2.11 - Undergraduate Thesis
Organization:FS - Faculty of Mechanical Engineering
Year:2025
Number of pages:XXII, 78 str.
PID:20.500.12556/RUL-167542 This link opens in a new window
UDC:615.478.73:616-072.1-71:004.057.2(043.2)
COBISS.SI-ID:22855757 This link opens in a new window
Publication date in RUL:27.02.2025
Views:332
Downloads:111
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Secondary language

Language:English
Title:Concurrent development of medical sterilizer and its IEC 61010 compliance
Abstract:
The thesis explores the concurrent development of a medical endoscope sterilizer and its compliance with IEC 61010. Unlike the traditional sequential approach, we applied concurrent engineering to optimize temperature regulation. A temperature controller was developed alongside software code, an electrical schematic, and a circuit for precise chamber temperature control. Testing confirmed compliance with ISO 15883 and successful completion of all IEC 61010 safety evaluations. By integrating verification early in the process, we reduced development time and minimized potential redesigns, fixes and/or adjustments. The use of concurrent engineering allowed simultaneous hardware and software validation, ensuring functional reliability and regulatory conformity. The findings demonstrate that real-time compliance assessment during development significantly accelerates certification while maintaining high apparatus safety and performance standards. This approach proves effective for optimizing complex medical apparatusses with precise controls and stringent regulatory compliance.

Keywords:device compliance, IEC 61010, measurements, concurrent development, sterilizers

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