Relevant bibliographies by topics / Safety device

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Safety device'

Author: Grafiati
Published: 4 June 2021
Last updated: 30 January 2023

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Journal articles on the topic "Safety device"

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Rathi, Vinay K., and Stacey T. Gray. "Device Safety." Otolaryngologic Clinics of North America 52, no. 1 (February 2019): 103–14. http://dx.doi.org/10.1016/j.otc.2018.08.013.

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GALLAURESI, BEVERLY ALBRECHT. "Device Safety." Nursing 29, no. 1 (January 1999): 31–40. http://dx.doi.org/10.1097/00152193-199901000-00015.

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SWAYZE, SONIA C. "Device Safety." Nursing 29, no. 5 (May 1999): 74–75. http://dx.doi.org/10.1097/00152193-199905000-00035.

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DILLARD, SHARON F. "Device Safety." Nursing 29, no. 7 (July 1999): 74. http://dx.doi.org/10.1097/00152193-199907000-00029.

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Raheja, Dev. "System Safety in Healthcare." Journal of System Safety 51, no. 3 (October 1, 2015): 11–12. http://dx.doi.org/10.56094/jss.v51i3.142.

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Unique Device Identification (UDI) is a recent development to protect patients from hazards in medical devices. The UDI relates to adverse event reporting, identifying and analyzing devices in use. Currently, hospitals are unable to report many adverse events because the device identification has to be manually located — and often, they are not easily readable, or the person reporting makes an error in reading or documenting the identification information. If a cardiac monitor malfunctions, it’s critical for the information in the adverse event report to match the manufacturer’s product identification system; otherwise, the adverse event may go unreported to U.S. Food and Drug Administration (FDA), and the device may not be recalled as soon as it should. The same urgency holds for a product recall sent from a manufacturer to the doctor, hospital or patient. An inability to identify the device affected by the recall could have potentially disastrous results for patients. In addition, if the device is for personal use, the user may not have access to information about the hazards other users of the device have experienced. With this new system, a user can easily search for hazards.
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Fehling, J. "Battery safety device." Journal of Power Sources 70, no. 1 (January 30, 1998): 163–64. http://dx.doi.org/10.1016/s0378-7753(97)84114-6.

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Paulsen, Benjamin Alexander, Sandra Henn, Georg Männel, and Philipp Rostalski. "Functional Safety Concept EGAS for Medical Devices." Current Directions in Biomedical Engineering 7, no. 2 (October 1, 2021): 739–42. http://dx.doi.org/10.1515/cdbme-2021-2189.

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Abstract For patient safety, it is important that a medical device can safely and reliably perform its intended purpose. The challenge in medical technology is that medical devices are heterogeneous systems and thus no widely applicable standard concepts for functional safety exist in medical technology. This is also reflected in the regulatory landscape, with its rather generally applicable standards. Patient safety is currently achieved by performing continuous risk management with an acceptable level of residual risk. Functional safety and its design concepts, as applied in other industries, have so far found little application in the field of medical technology. In this paper, the automotive safety concept "EGAS" is analyzed with regard to its applicability for medical devices. Based on the investigated example of a medical ventilator, important parallels were found between the automotive and the medical device sector, indicating the possibility of successfully applying the EGAS safety concept to medical devices.
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Bisht, Yogesh Singh. "Device to Device based Women Safety System." International Journal for Research in Applied Science and Engineering Technology 9, no. VI (June 14, 2021): 620–25. http://dx.doi.org/10.22214/ijraset.2021.35045.

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Device-to-device (D2D) communication, which offers ultra-low latency for user communication, is projected to play a large role in future cellular networks. This new mode could work in either licensed or unlicensed spectrum. It's a fresh take on the classic cellular communication model. Its advantages, however, come with a slew of technological and financial difficulties that must be addressed before it can be fully integrated into the cellular ecosystem. This paper discusses the main characteristics of D2D communication and how we can use this to build Human Safety Device.
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Bhatia, Nisha, and Krishna Kumari Meka. "Acceptability, Safety and Uptake of Transcesarean Intrauterine Contraceptive Device." Indian Journal of Obstetrics and Gynecology 7, no. 4 (P-2) (2019): 605–12. http://dx.doi.org/10.21088/ijog.2321.1636.7419.6.

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R., Balamurugan, and Muruganantham T. "Women Safety Ensurance Device." IJARCCE 8, no. 6 (June 30, 2019): 22–24. http://dx.doi.org/10.17148/ijarcce.2019.8604.

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Dissertations / Theses on the topic "Safety device"

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Doran, Neslihan Iclal 1977. "Evaluation of a digital communication device for railroad worker safety." Thesis, Massachusetts Institute of Technology, 2005. http://hdl.handle.net/1721.1/28909.

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Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Aeronautics and Astronautics; and, (S.M.)--Massachusetts Institute of Technology, Engineering Systems Division, Technology and Policy Program, 2005.
Includes bibliographical references (leaf 65).
This thesis documents the testing of a prototype of a smartphone to be used by roadway workers and dispatchers that was based in a wireless data link service. The main purpose of using a smartphone in railroad communications is to eliminate errors due to radio and pronunciation deficiencies. Previous studies analyzed the communication environment of the dispatcher in order to address questions based upon data link becoming a means for sending and receiving information in railroad operations. These studies have examined what kind of information is appropriate for each medium (voice and visual), and by what criteria a dispatcher will select which communication medium. Building on these studies, this work presents a comparison between a radio and data link mediums for a long communication of a characteristic type: assignment of a form D. This thesis reports on the on site testing of the data link system which proved to be useful and efficient in certain aspects of railroad applications. The new system was faster and more effective than the radio communication when used to convey long messages such as filling out Form Ds. The radio communication was faster than the datalink for confirmation communications that only require yes/no answers. One reason for this difference appears to be the users' unfamiliarity with the device. The time to convey short messages could also be reduced after the users become more proficient with the new system. The document also includes an analysis of the regulatory challenges that the new system would bring. A list or recommendations for the new regulations are presented at the end of the report.
by Neslihan Iclal Doran.
S.M.
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Song, Qingyang S. M. Massachusetts Institute of Technology. "A system theoretic approach to design safety into medical device." Thesis, Massachusetts Institute of Technology, 2012. http://hdl.handle.net/1721.1/76510.

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Thesis (S.M. in Engineering and Management)--Massachusetts Institute of Technology, Engineering Systems Division, System Design and Management Program, 2012.
Cataloged from PDF version of thesis.
Includes bibliographical references (p. 65-66).
The goal of this thesis is to investigate and demonstrate the application of a systems approach to medical device safety in China. Professor Leveson has developed an accident modeling framework called STAMP (Systems Theoretic Accident Modeling and Processes.) Traditional accident models typically focus on component failure; in contrast, STAMP includes interactions between components as well as social, economic, and legal factors. In this thesis, the accident of the artificial heart at a level II hospital in China was used as a test case to study whether Causal Analysis based on STAMP (CAST) is used to outline the interactions between the different medical device system components, identify the safety control structure in place, and understand how this control structure failed to prevent artificial heart accident in a Chinese hospital. The analysis suggested that further changes might be necessary to protect the Chinese public and so, based on the results of the CAST, a new set of systemic recommendations was proposed.
by Qingyang Song.
S.M.in Engineering and Management
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Shuja, Sana. "Formal Verification Techniques for Safety Critical Medical Device Software Control." Diss., North Dakota State University, 2016. http://hdl.handle.net/10365/25736.

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Safety-critical medical devices play an important role in improving patients health and lifestyle. Faulty behaviors of such devices can cause harm or even death. Often these faulty behaviors are caused due to bugs in software programs used for digital control of the device. We present a formal veri cation methodology that can be used to check the correctness of object code programs that implement the safety-critical control functions of these medical devices. Our methodology is based on the theory of Well-Founded Equivalence Bisimulation (WEB) re nement, where both formal speci cations and implementations are treated as transition systems. First, we present formal speci cation model for the medical device. Second, we develop correctness proof obligations that can be applied to validate object code programs used in these devices. Formal methods are not widely employed for the veri cation of safety critical medical devices. However, using our methodology we were able to bridge the gap between two very important phases of software life cycle: speci cation and veri cation.
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Armsby, Pauline M. "An intelligent pedestrian device : social, psychological and other issues of feasibility." Thesis, Middlesex University, 1996. http://eprints.mdx.ac.uk/9847/.

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An Intelligent Pedestrian Device (IPD) is a new concept in pedestrian safety. It is defined as a microprocessor based information device which detects the approach of oncoming vehicles and informs the pedestrian whether or not it is safe to cross. IPDs could be portable or fixed to a roadside station. They could help reduce pedestrian accidents, which cost £2681 million in the UK in 1994. This study aims to assess whether the concept is socially acceptable and what the design criteria might be. A study of social acceptance involved group interviews of 5-10 participants with 84 pedestrians in five categories: adults aged 18-60, elderly aged 65+, visually restricted, parents of children aged 5-9 and children aged 10-14. The results suggest that vulnerable pedestrians are more positive about the device than the more able-bodied. Theories that may help explain this are discussed and it is concluded that, with education and marketing, the IPD could gain a degree of social acceptance. Observation of more than 900 pedestrian crossing movements at four different sites showed a range of behaviours, and that people often take risks in order to reduce delay. IPDs will require pedestrians to change some of their behaviours, especially those that are risky. Legal acceptance will demand high levels of costly product research and development, and a portable device will not be technologically feasible until well into the next century. However, the wider social benefits of IPDs may be worth the costs. An outline of design criteria for basic and sophisticated portable IPDs is given, and alternative functions are suggested. It is recommended that further work concentrate on developing software and hardware for fixed modes of IPD. It is concluded that, ultimately, acceptance will probably depend on whether Government decides that the IPD has a place in the road environment of the future.
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Hinrichs, Saba. "A systems approach to improving patient safety through medical device purchasing." Thesis, University of Cambridge, 2010. https://www.repository.cam.ac.uk/handle/1810/238973.

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The purchase of medical devices involves engaging various stakeholders as well as balancing clinical, technical and financial requirements. Failure to consider these requirements can lead to wider consequences in the delivery of care. This study first builds a general knowledge base of current purchasing practice in a sample of NHS Trusts, which confirms the direction and guidance given by policy documents and literature as to the extent of the challenges faced by purchasing stakeholders. This then leads to an analysis to identify inefficiencies in the purchasing process, and how such practice can lead to risks in the delivery of care. These risks range from injury to individuals, impacts to the healthcare delivery service, and financial and litigation risks. Finally, a framework that highlights these potential risks in the life-cycle of medical devices in hospitals is presented. Key policy guidance has encouraged both researchers and implementers of healthcare services to approach patient safety from a systems perspective, acknowledging that medical device errors are not only directly related to device design, but to the design of the healthcare delivery service system in which the device operates. Little evidence exists of successfully applying systems approaches specifically to medical device purchasing practice. Medical device purchasing, because of its implications to patient safety on the one hand, and the uniqueness of the healthcare context, requires a unique approach. By demonstrating the influence of purchasing practice to service delivery and patient care, the thesis made is that taking a holistic systems approach is one method to improve device purchasing practice, and hence influence better care.
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Oriol, Hoyos Nicolas 1973. "Design and evaluation of a communications device to enhance railroad worker safety." Thesis, Massachusetts Institute of Technology, 2000. http://hdl.handle.net/1721.1/89281.

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Lindholm, Christin. "Software development and risk management in the safety critical medical device domain /." Lund : Department of Computer Science, Lund University, 2009. http://www.lu.se/o.o.i.s?id=12683&postid=1304138.

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Guignard, Thibaut Xavier. "Implementation of a stable power assist device." Thesis, Georgia Institute of Technology, 2000. http://hdl.handle.net/1853/17059.

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Doyle, Marc. "Comprehending the Safety Paradox and Privacy Concerns with Medical Device Remote Patient Monitoring." Diss., NSUWorks, 2019. https://nsuworks.nova.edu/gscis_etd/1090.

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Medical literature identifies a number of technology-driven improvements in disease management such as implantable medical devices (IMDs) that are a standard treatment for candidates with specific diseases. Among patients using implantable cardiac defibrillators (ICD), for example, problems and issues are being discovered faster compared to patients without monitoring, improving safety. What is not known is why patients report not feeling safer, creating a safety paradox, and why patients identify privacy concerns in ICD monitoring. There is a major gap in the literature regarding the factors that contribute to perceived safety and privacy in remote patient monitoring (RPM). To address this gap, the research goal of this study was to provide an interpretive account of the experience of RPM patients. This study investigated two research questions: 1) How did RPM recipients perceive safety concerns?, and 2) How did RPM recipients perceive privacy concerns? To address the research questions, in-depth, semi-structured interviews were conducted with six participants to explore individual perceptions in rich detail using interpretative phenomenological analysis (IPA). Four themes were identified and described based on the analysis of the interviews that include — comfort with perceived risk, control over information, education, and security — emerged from the iterative review and data analysis. Participants expressed comfort with perceived risk, however being scared and anxious were recurrent subordinate themes. The majority of participants expressed negative feelings as a result of an initial traumatic event related to their devices and lived in fear of being shocked in inopportune moments. Most of these concerns stem from lack of information and inadequate education. Uncertainties concerning treatment tends to be common, due to lack of feedback from ICD RPM status. Those who knew others with ICD RPM became worrisome after hearing about incidences of sudden cardiac death (SCD) when the device either failed or did not work adequately to save their friend’s life. Participants also expressed cybersecurity concerns that their ICD might be hacked, maladjusted, manipulated with magnets, or turned off. They believed ICD RPM security was in place but inadequate as well as reported feeling a lack of control over information. Participants expressed wanting the right to be left alone and in most cases wanted to limit others’ access to their information, which in turn, created conflict within families and loved ones. Geolocation was a contentious node in this study, with most of participants reporting they did not want to be tracked under any circumstances. This research was needed because few researchers have explored how people live and interact with these newer and more advanced devices. These findings have implications for practice relating to RPM safety and privacy such as identifying a gap between device companies, practitioners, and participants and provided directions for future research to discover better ways to live with ICD RPM and ICD shock.
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August, Sharon. "An objective approach to adapted input device prescription and customization /." Thesis, McGill University, 1991. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=59980.

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Microcomputer technology and the provision of alternative data entry devices offers numerous opportunities for physically disabled individuals to integrate into work and school settings. For therapists specializing in adapted access one of the main challenges involves prescribing and customizing suitable input devices since objective procedures to facilitate this process are lacking. The two papers presented in this thesis aimed to respond to this limitation. In the first paper the adapted access process was viewed within the context of a human factors model. A critical review of the literature relating specific human factors criteria (e.g. digit loading) to ergonomic solutions (e.g. input/output efficiency) substantiated clinical approaches to adapted device prescription and customization. Two case studies were used to illustrate the application of this approach to physically disabled individuals. The second paper investigated therapists' abilities to judge the mechanical characteristics of switches. Objective data characterizing the activation force-displacement trajectories for eight commonly used adapted switches were collected and compared to clinicians' subjective evaluation of the same characteristics. The major finding was that although therapists' subjective estimates of activation force and displacement were reasonably good there were specific areas of weakness that should be rectified with quantitative, objective data. It is anticipated that these two papers will enhance the application of microcomputer usage for physically disabled individuals.
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Books on the topic "Safety device"

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Medical device safety: The regulation of medical devices for public health and safety. Bristol: Institute of Physics Pub., 2002.

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Southern Building Code Congress International. Standard amusement device code. Birmingham, Ala: Southern Building Code Congress International, 1985.

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United States. Food and Drug Administration. FDA device inspections manual. Arlington, VA: Washington Business Information, 1994.

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Eeckhoven, Eddie F. J. van., ed. Medical device vigilance/monitoring: European device directives compliance. Buffalo Grove, Ill: Interpharm Press, 1997.

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Heller, Mark A. Guide to medical device regulation. Washington, DC: Thompson Pub. Group, 1997.

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Heller, Mark A. Guide to medical device regulation. Washington, D.C: Thompson Pub. Group, 1993.

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Schoenmakers, C. C. W. CE marking for medical devices: A handbook to the medical devices directives : Medical Device Directive 93/42/EEC : the Active Implantable Medical Device Directive 90/396/EEC. New York, NY: Standards Information Network/IEEE Press, 1997.

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Medical Device Amendments of 1992. [Washington, D.C.?: U.S. G.P.O., 1992.

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McIlroy, Trevor. Safety critical programmable logic device design using VHDL (military application). [s.l: The Author], 2004.

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Medical device design and regulation. Milwaukee, Wis: ASQ Quality Press, 2011.

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Book chapters on the topic "Safety device"

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Gad, Shayne C. "Device Safety Evaluation." In Safety Evaluation of Pharmaceuticals and Medical Devices, 91–112. Boston, MA: Springer US, 2010. http://dx.doi.org/10.1007/978-1-4419-7449-5_7.

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Dilip Kumar, S., A. Archana, S. Sri Dharshini, and K. Peridev. "Smart Women Safety Device." In Advances in Automation, Signal Processing, Instrumentation, and Control, 595–602. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-15-8221-9_52.

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Siddharth, P. N., and C. T. Justus Panicker. "Fool Proof Two-Wheeler Safety Device." In Lecture Notes in Electrical Engineering, 939–49. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-15-9019-1_79.

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Arabo, Abdullahi, Qi Shi, and Madjid Merabti. "Dynamic Device Configuration in Ubiquitous Environments." In Global Security, Safety, and Sustainability, 263–73. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-15717-2_28.

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Doyle, Peter A. "Improving Safety of Medical Device Use Through Training." In Safety of Health IT, 241–52. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-31123-4_19.

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Zusterzeel, Robbert. "Safety and Effectiveness of Medical Device Therapy." In Advances in Experimental Medicine and Biology, 107–21. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-77932-4_7.

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Kim, Cheolgi, Mu Sun, Heechul Yun, and Lui Sha. "A Medical Device Safety Supervision over Wireless." In Reliable and Autonomous Computational Science, 21–40. Basel: Springer Basel, 2010. http://dx.doi.org/10.1007/978-3-0348-0031-0_2.

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‘Aqilah Arshad, Siti Ramlah, Zuhanis Mansor, Siti Marwangi Mohamad Maharum, and Izanoordina Ahmad. "Women Safety Device with Real-Time Monitoring." In Advanced Structured Materials, 273–82. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-92964-0_27.

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Benet, Albert Farré. "A Risk Driven Approach to testing Medical Device Software." In Advances in Systems Safety, 157–68. London: Springer London, 2010. http://dx.doi.org/10.1007/978-0-85729-133-2_10.

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Agarwal, Madhu, Simantika Saha, Soumyadeep Pandit, Prasenjit Sarkar, Shreya Shree Das, and Subhojit Dawn. "Smart Wearable Safety Device: A Wearable Anti-Assault and Location Tracking Device." In Algorithms for Intelligent Systems, 591–95. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-2109-3_54.

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Conference papers on the topic "Safety device"

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Moodbidri, Akash, and Hamid Shahnasser. "Child safety wearable device." In 2017 International Conference on Information Networking (ICOIN). IEEE, 2017. http://dx.doi.org/10.1109/icoin.2017.7899531.

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Rai, Utsav, Kashish Miglani, Aman Saha, Bismita Sahoo, and M. Vergin Raja Sarobin. "ReachOut Smart Safety Device." In 2018 6th Edition of International Conference on Wireless Networks & Embedded Systems (WECON). IEEE, 2018. http://dx.doi.org/10.1109/wecon.2018.8782071.

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Gautam, Chandan, Abhishek Patil, Akanksha Podutwar, Maitreyee Agarwal, Pranali Patil, and Apurva Naik. "Wearable Women Safety Device." In 2022 IEEE Industrial Electronics and Applications Conference (IEACon). IEEE, 2022. http://dx.doi.org/10.1109/ieacon55029.2022.9951850.

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Ranjeeth, Bannuru, B. Srinivasa Reddy, Y. Manoj Kumar Reddy, S. Suchitra, and B. Pavithra. "Smart Child Safety Wearable Device." In 2020 International Conference on Electronics and Sustainable Communication Systems (ICESC). IEEE, 2020. http://dx.doi.org/10.1109/icesc48915.2020.9156001.

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Jo, Sung-Gu. "Wearable Monitoring Device in Security." In Security, Reliability, and Safety 2015. Science & Engineering Research Support soCiety, 2015. http://dx.doi.org/10.14257/astl.2015.93.06.

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Viswanath, Nandita, Naga Vaishnavi Pakyala, and G. Muneeswari. "Smart foot device for women safety." In 2016 IEEE Region 10 Symposium (TENSYMP ). IEEE, 2016. http://dx.doi.org/10.1109/tenconspring.2016.7519391.

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Charrière, Karine, Jean-Francois Manceau, Pascal Morel, Véronique Bourcier, Wilfrid Boireau, Lionel Pazart, and Bruno Wacogne. "Test Device for Blood Transfusion Safety." In 11th International Conference on Biomedical Electronics and Devices. SCITEPRESS - Science and Technology Publications, 2018. http://dx.doi.org/10.5220/0006635702060211.

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Chitkara, Divya, Nipun Sachdeva, and Yash Dev Vashisht. "Design of a women safety device." In 2016 IEEE Region 10 Humanitarian Technology Conference (R10-HTC). IEEE, 2016. http://dx.doi.org/10.1109/r10-htc.2016.7906858.

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Yang, Jiajun. "Electric power safety intelligent monitoring device." In XVI INTERNATIONAL CONFERENCE ON LUMINESCENCE AND LASER PHYSICS DEVOTED TO THE 100TH ANNIVERSARY OF IRKUTSK STATE UNIVERSITY. Author(s), 2019. http://dx.doi.org/10.1063/1.5089060.

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Johri, Prashant, Vishnu Sharma, Varuna Gupta, and Vishwadeepak Singh Baghela. "Smart Tracker Device for Women Safety." In 2021 3rd International Conference on Advances in Computing, Communication Control and Networking (ICAC3N). IEEE, 2021. http://dx.doi.org/10.1109/icac3n53548.2021.9725611.

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Reports on the topic "Safety device"

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Fowler, Steven E. Safety and Arming Device Design Principles. Fort Belvoir, VA: Defense Technical Information Center, May 1999. http://dx.doi.org/10.21236/ada363924.

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Gillilan, Justin. Radiation-Generating Device Safety Self-Study. Office of Scientific and Technical Information (OSTI), January 2022. http://dx.doi.org/10.2172/1840863.

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Robinson, Charles H., Robert H. Wood, Andrew Bayba, and David Hollingsworth. MEMS Safety and Arming Device for OICW. Fort Belvoir, VA: Defense Technical Information Center, August 2001. http://dx.doi.org/10.21236/ada386187.

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Dirks, Richard. Common Precision Munitions Safety & Arming Device. Fort Belvoir, VA: Defense Technical Information Center, April 2001. http://dx.doi.org/10.21236/ada386214.

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Zhen, Guo, Maimaitili Aisha, Wang Kai, Kaheerman Kadeer, and Cheng Xiaojiang. The efficacy and safety of flow-diverting device and coil embolization for intracranial aneurysms: a meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, December 2020. http://dx.doi.org/10.37766/inplasy2020.12.0108.

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US ARMY ARDEC. Safety Design Requirements for Active Hazard Mitigation Device (AHMD) Employed to Address Fast and Slow Cook-off Thermal Threats. Fort Belvoir, VA: Defense Technical Information Center, December 2014. http://dx.doi.org/10.21236/ada617010.

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Lukezich, S. J. Sealed source and device design safety testing. Technical report on the findings of task 4. Investigation of a failed brachtherapy needle applicator. Office of Scientific and Technical Information (OSTI), May 1997. http://dx.doi.org/10.2172/481869.

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Tangm, Liyan, Haiying Teng, and Zhong Wang. Efficacy and Safety of An External Combined Occipital and Trigeminal Neurostimulation (eCOT-NS) Device for Migraine: A Systematic Review and Meta-Analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, November 2022. http://dx.doi.org/10.37766/inplasy2022.11.0074.

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Benac, D. J., and H. C. Burghard. Sealed source and device design safety testing: Technical report on the findings of task 4 -- Investigation of failed Nitinol brachytherapy wire. Volume 2. Office of Scientific and Technical Information (OSTI), March 1996. http://dx.doi.org/10.2172/226076.

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Benac, D. J., and F. A. Iddings. Sealed source and device design safety testing. Volume 4: Technical report on the findings of Task 4, Investigation of sealed source for paper mill digester. Office of Scientific and Technical Information (OSTI), October 1995. http://dx.doi.org/10.2172/137419.

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