No results for "Category:Regulation of medical devices" (auto) in titles.

Suggestions for article titles:

1. Medical device: COUNCIL DIRECTIVE 93/42/EEC of 14 June 1993 concerning medical devices defines a ‘medical device’ as: any instrument, apparatus, appliance, material or other article, whether used alone or in combination, including the software necessary for its proper application intended ... [100%] 2023-12-31 [Medical equipment]
2. Medical device: A medical device is any device intended to be used for medical purposes. Significant potential for hazards are inherent when using a device for medical purposes and thus medical devices must be proved safe and effective with reasonable assurance before ... (Medicine) [100%] 2023-10-31 [Medical devices] [Health care]...
3. Medical device: Any equipment meant to be used for medical reasons is considered a medical device. Since utilizing a device for medical purposes carries a significant risk, medical devices must be demonstrated to be safe and effective with a high degree of ... [100%] 2024-03-18 [Medical devices] [Health care]...
4. Medical device: A medical device is any device intended to be used for medical purposes. Significant potential for hazards are inherent when using a device for medical purposes and thus medical devices must be proved safe and effective with reasonable assurance before ... (Device to be used for medical purposes) [100%] 2024-07-22 [Medical devices] [Health care]...
5. Medical Devices Directive: The Medical Device Directive—Council Directive 93/42/EEC of 14 June 1993 concerning medical devices—is intended to harmonise the laws relating to medical devices within the European Union. The MD Directive is a 'New Approach' Directive and consequently ... [89%] 2024-04-21 [European Union directives] [European Union technology policy]...
6. Expert Review of Medical Devices: Expert Review of Medical Devices is a monthly peer-reviewed medical journal covering research on the clinical use of devices. It was established in 2004 and is published by Informa. (Medicine) [85%] 2023-11-10 [Engineering journals]
7. Devices and Desires: Devices and Desires is a 1989 detective novel by English writer P. D. (1989 Dalgliesh novel by P. D. James) [83%] 2024-01-09 [1989 British novels] [Novels by P. D. James]...
8. Which Medical Device: Which Medical Device is a review site for medical devices with reviews, medical device news and videos of medical procedures. Users can rate and review medical devices listed on the website, or suggest devices for inclusion and review. (Medicine) [81%] 2023-11-29 [Medical websites]
9. Medical device design: Due to the many regulations in the industry, the design of medical devices presents significant challenges from both engineering and legal perspectives. The United States medical device industry is one of the largest markets globally, exceeding $110 billion annually. (Medicine) [81%] 2024-01-01 [Medical devices]
10. Medical device manufacturing: Template:Globalize/US Medical device manufacturing, as the name suggests, refers to the production of medical devices. Due to the large amount of regulations in the industry, the production of medical devices presents significant challenges from both engineering and legal ... (Medicine) [81%] 2023-12-20 [Medical devices]
11. Medical device connectivity: Medical device connectivity is the establishment and maintenance of a connection through which data is transferred between a medical device, such as a patient monitor, and an information system. The term is used interchangeably with biomedical device connectivity or biomedical ... (Medicine) [81%] 2024-01-01 [Medical devices] [Health informatics]...
12. Medical device hijack: A medical device hijack (also called medjack) is a type of cyber attack. The weakness they target are the medical devices of a hospital. (Medicine) [81%] 2024-01-01 [Medical devices] [Computer security exploits]...
13. Medical device reporting: Medical device reporting (MDR) is the procedure for the Food and Drug Administration to get significant medical device adverse events information from manufacturers, importers and user facilities, so these issues can be detected and corrected quickly, and the same lot ... [81%] 2024-04-19 [Food and Drug Administration] [Regulation of medical devices]...
14. Medical device design: Due to the many regulations in the industry, the design of medical devices presents significant challenges from both engineering and legal perspectives. The United States medical device industry is one of the largest markets globally, exceeding $110 billion annually. [81%] 2024-07-22 [Medical devices] [Product design]...
15. Medical Devices Park, Hyderabad: Medical Devices Park, Hyderabad is a medical devices industrial estate located in Hyderabad, Telangana, India . The largest such Park in India spread over 250 acres. (Medicine) [77%] 2024-01-01 [Biotechnology]
16. Single-use medical devices: Single-use medical devices include any medical equipment, instrument or apparatus having the ability to only be used once in a hospital or clinic and then disposed. The Food and Drug Administration defines this as any device entitled by its ... (Medicine) [77%] 2024-01-01 [Medical devices]
17. Agency for Medicinal Products and Medical Devices of the Republic of Slovenia: Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (Slovene: Javna agencija Republike Slovenije za zdravila in medicinske pripomočke; acronym: JAZMP) is a regulatory agency of the Republic of Slovenia competent for medicinal products and medical devices ... [74%] 2024-01-01 [Medical and health organizations based in Slovenia] [Organizations established in 2007]...
18. Devizes: Devizes (/dɪˈvaɪzɪz/) is a market town and civil parish in Wiltshire, England. It developed around Devizes Castle, an 11th-century Norman castle, and received a charter in 1141. (Town in Wiltshire, England) [72%] 2024-04-21 [Devizes] [Market towns in Wiltshire]...
19. Safe Medical Device Amendments of 1990: Safe Medical Device Amendments of 1990 or Safe Medical Devices Act sanctioned progressive reporting and tracking rules for medical devices classified by the Medical Device Regulation Act. The Act mandates reporting requirements by medical device manufacturers regarding adverse safety events ... [72%] 2024-01-01 [101st United States Congress] [United States federal health legislation]...
20. Safe Medical Device Amendments of 1990: Safe Medical Device Amendments of 1990 or Safe Medical Devices Act sanctioned progressive reporting and tracking rules for medical devices classified by the Medical Device Regulation Act. The Act mandates reporting requirements by medical device manufacturers regarding adverse safety events ... (Medicine) [72%] 2024-01-01 [Health care quality]