Definition Medical Device Adverse Event

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What is a Serious Adverse Event? | FDA

https://www.fda.gov/safety/reporting-serious-problems-fda/what-serious-adverse-event

Report if the adverse event resulted in a substantial disruption of a person's ability to conduct normal life functions, i.e., the adverse event resulted in a significant, persistent or permanent change, impairment, damage or disruption in the patient's body function/structure, physical activities and/or … See more

MDR Adverse Event Codes | FDA

https://www.fda.gov/medical-devices/mandatory-reporting-requirements-manufacturers-importers-and-device-user-facilities/mdr-adverse-event-codes

The FDA Medical Device Report (MDR) adverse event codes are collectively a system of codes, terms, and definitions used to describe and categorize medical device adverse …

Adverse Event Reporting for Medical Devices Under …

https://www.fda.gov/medical-devices/coronavirus-covid-19-and-medical-devices/adverse-event-reporting-medical-devices-under-emergency-use-authorization-eua-or-discussed-covid-19

Medical device reporting under 21 CFR Part 803 generally requires reporting of deaths, serious injuries, and malfunctions that have, may have, or would be likely to …

Medical Device Reporting (MDR): How to Report Medical …

https://www.fda.gov/medical-devices/medical-device-safety/medical-device-reporting-mdr-how-report-medical-device-problems

Patients, healthcare professionals and consumers who find a problem related to a medical device are encouraged to report medical device adverse events or product problems to …

Device Adverse Event Overview - Food and Drug …

https://open.fda.gov/apis/device/event/

The openFDA device adverse event API returns data from Manufacturer and User Facility Device Experience (MAUDE), an FDA dataset that contains medical device …

MDR - Article 2 - Definitions - Medical Device Regulation

https://www.medical-device-regulation.eu/2019/07/10/mdr-article-2-definitions/

(57) ‘adverse event’ means any untoward medical occurrence, unintended disease or injury or any untoward clinical signs, including an abnormal laboratory …

eCFR :: 21 CFR Part 803 -- Medical Device Reporting

https://www.ecfr.gov/current/title-21/chapter-I/subchapter-H/part-803

( 1) An event that user facilities become aware of that reasonably suggests that a device has or may have caused or contributed to a death or serious injury or ( 2) An event that …

Adverse event or incident relating to a medical device …

https://www.lawinsider.com/dictionary/adverse-event-or-incident-relating-to-a-medical-device

Adverse event or incident relating to a medical device means any malfunction of the medical device, performance failures, absence or impaired efficacy of the medical …

HSA | Adverse events reporting of medical devices

https://www.hsa.gov.sg/medical-devices/adverse-events

Any adverse event (AE), which meets the three basic reporting criteria listed below, is considered as a reportable adverse event: An AE (or potential AE) has occurred. The …

IDE Definitions and Acronyms | FDA

https://www.fda.gov/medical-devices/investigational-device-exemption-ide/ide-definitions-and-acronyms

Investigational device is a device, including a transitional device, that is the object of an investigation. Investigational device exemption (IDE) IDE refers to the …

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