Sökning: "medicintekniska produkter"
Visar resultat 11 - 15 av 66 uppsatser innehållade orden medicintekniska produkter.
11. MDR’s Impact on Standards Usages and the Relevance for In-house Production of Medical Devices
Kandidat-uppsats, KTH/Medicinteknik och hälsosystemSammanfattning : The current regulation for Medical Devices (MDR) entered into force on 26 May 2021, which has entailed major changes to relevant legislation for in-house production of medical devices in healthcare. The relevance for updating existing, or the development of new standards is currently not well documented and determined and the aim of this report is to make recommendations for how the development of standards may be improved and how departments of medical technology (DMT) in practice apply standards at in-house production of medical devices. LÄS MER
12. Quality Management Systems in Healthcare : “Implementation of the Medical Device Regulation”
Master-uppsats, KTH/Skolan för industriell teknik och management (ITM)Sammanfattning : This study investigated how a QMS that is compliant with the Medical Device Regulation (MDR) can be constructed and what the most important aspects are when creating a functional QMS at a Swedish hospital. QMS:s are a fundamental part of a healthcare organization and are used to ensure safe and secure patient care. LÄS MER
13. Circular Economy in Single-Use Medical Device Industry : Barriers, Enablers and Design Tool
Master-uppsats, KTH/Skolan för industriell teknik och management (ITM)Sammanfattning : Healthcare waste is on an all-time high with single-use devices being one of the largest contributors. With the onset of Covid-19, this issue has become highly visible and has led to global concerns being raised around the environmental footprint of the healthcare sector and the need to reduce the waste generated by shifting away from single-use devices. LÄS MER
14. Evaluating the Implementation and Results of EU 2017/745
Master-uppsats, KTH/Medicinteknik och hälsosystemSammanfattning : The new regulation on medical devices, EU 2017/745, came into force in May 2021 meaning that all economic operators in the industry need to adhere to new, stricter requirements. As there is yet no common practice on how to implement and comply with the new requirements, many struggles with this. LÄS MER
15. Cirkulära metallflöden i medicinteknisk utrustning
Kandidat-uppsats, Uppsala universitet/Institutionen för geovetenskaperSammanfattning : I denna studie undersöktes cirkulära metallflöden i medicinteknik på Akademiska sjukhuset i Uppsala och Region Uppsala. Syftet var att kartlägga och undersöka kritiska metaller i utvald medicinteknisk utrustning. Återvinningen av metaller i utrustningen på Akademiska sjukhuset undersöktes. LÄS MER