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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.
The FDA provides a database for reporting of adverse medical device events called the Manufacturer and User Facility Device Experience Database (MAUDE)[1]. The data consist of voluntary reports since June 1993, user facility reports since 1991, distributor reports since 1993, and manufacturer reports since August 1996, and is open for public view.
Global Medical Device Nomenclature (GMDN) is a system of internationally agreed generic descriptors used to identify all medical device products. This nomenclature is a naming system for products which include those used for the diagnosis, prevention, monitoring, treatment or alleviation of disease or injury in humans.
First Databank (FDB) is a major provider of drug and medical device databases that help inform healthcare professionals to make decisions. [1] FDB partners with information system developers to deliver useful medication- and medical device-related information to clinicians, business associates, and patients.
Wolf Martin Garber (May 18, 1922 – October 17, 2019), known professionally as Bill Macy, was an American television, film and stage actor known for his role in the CBS television series Maude (1972–1978).
The Maude Abbott Medical Museum (French: Musée Médical Maude Abbott) is a medical museum located at McGill University in Montreal, Quebec, Canada. The museum is named after Canadian doctor Maude Abbott , who served as its curator in the late 19th century.
Westerns, fantasies, outer space and even fast fashion are influencing the baby boy names of 2025, making certain names even more popular.
A similar database is the Global Unique Device Identification Database (GUDID) of the FDA. As a key to EUDAMED, the MDR introduces the Basic UDI-DI as unique device identifier. A medical device (including system- and procedure packs and IVD) needs to have an assigned Basic UDI-DI and needs to be registered in the UDI/Device part of EUDAMED.