Essays about: "Medical device manufacturers"

Showing result 1 - 5 of 10 essays containing the words Medical device manufacturers.

1. 1. Exploring IoT Security Threats and Forensic Challenges: A LiteratureReview and Survey Study

   University essay from Linnéuniversitetet/Institutionen för datavetenskap och medieteknik (DM)

   Author : Abdulrahman Al Allaf; Waseem Totonji; [2023]
   Keywords : Internet of Things; IoT security; IoT threats; IoT attacks; Digital forensics; IoT forensic; IoT forensic challenges; Cloud forensics; Network forensics;

   Abstract : Internet of Things (IoT) devices have increased rapidly in recent years, revolutionizing many industries, including healthcare, manufacturing, and transportation, and bringing benefits to both individuals and industries. However, this increase in IoT device usage has exposed IoT ecosystems to numerous security threats and digital forensic challenges. READ MORE

3. 2. Circular Economy in Single-Use Medical Device Industry : Barriers, Enablers and Design Tool

   University essay from KTH/Skolan för industriell teknik och management (ITM)

   Author : Akshat Jain; [2022]
   Keywords : ;

   Abstract : 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. READ MORE

4. 3. MDR 2017/745 - New EU Regulation for Medical Devices: A Process Description for EHR Manufacturers on How to Fulfill the Regulation

   University essay from KTH/Medicinteknik och hälsosystem

   Author : Frida Germundsson; Nicole Kvist; [2020]
   Keywords : MDR; regulation; process description; EHR system; CE mark; medical technology;

   Abstract : On the 26th of May 2021 the new regulation for medical devices, MDR 2017/745, will come into force. The underlying incentives to go from the medical device directive (MDD 93/42/EEC) to MDR are a series of adverse events involving medical devices. READ MORE

5. 4. Evaluating the Compliance Re-Certification Efficiency Enabled by the AMASS Platform for Medical Devices

   University essay from Mälardalens högskola/Akademin för innovation, design och teknik

   Author : Aleksandër Pulla; Antonela Bregu; [2020]
   Keywords : AMASS project; certification; re-certification; efficiency; medical devices; ISO 14971; NBRG Consensus paper; reuse; standard; tool-chain; metrics; directives; regulations;

   Abstract : The certification of systems in the medical domain aims to ensure that a system is acceptably safein order to bear the CE mark. Such process is exhaustive, expensive, time-consuming and safety-critical.Medical devices shall be re-certified under Medical Device Regulations. READ MORE

6. 5. Advanced Clinical Data Processing: A Predictive Maintenance Model for Anesthesia Machines

   University essay from KTH/Tillämpad fysik

   Author : Kerim Numanovic; [2020]
   Keywords : Appled Physics; Tillämpad fysik;

   Abstract : The maintenance of medical devices is of great importance to ensure that the devices are stable, well-functioning, and safe to use. The current method of maintenance, which is called preventive maintenance, has its advantages but can be problematic both from an operators’ and a manufacturers’ side. READ MORE