Medical device reporting
id:
medical-device-reporting-274-12451540
title:
Medical device reporting
text:
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 of that product may be recalled. Consumers and health professionals report any adverse event caused by the device to MedWatch program for reporting significant adverse events or product problems with medical products.
brand slug:
wiki
category slug:
encyclopedia
description:
original url:
https://en.wikipedia.org/wiki/Medical_device_reporting
date created:
date modified:
2022-11-04T11:01:48Z
main entity:
{"identifier":"Q6806506","url":"https://www.wikidata.org/entity/Q6806506"}
image:
fields total:
13
integrity:
13