maude fda - Resultados da busca Yahoo Search

Resultado da Busca

www.accessdata.fda.gov › cfdocs › cfmaudeManufacturer and User Facility Device Experience (MAUDE) Database

www.accessdata.fda.gov › cfdocs › cfmaude
- Em cache
30 de abr. de 2024 · MAUDE is a searchable database of adverse events involving medical devices over the last ten years. Users can search on product, problem, event type, manufacturer, model number, report number and other fields to find reports submitted by mandatory or voluntary reporters.
- Maude
  The MAUDE database houses medical device reports submitted...
- Standards
  This database provides the most up-to-date list of voluntary...
- CLIA
  Gostaríamos de exibir a descriçãoaqui, mas o site que você...
- Adverse Events
  The Manufacturer and User Facility Device Experience (MAUDE)...
www.fda.gov › medical-devices › mandatory-reportingAbout Manufacturer and User Facility Device Experience (MAUDE)

www.fda.gov › medical-devices › mandatory-reporting
- Em cache
23 de out. de 2023 · MAUDE (Manufacturer and User Facility Device Experience) contains reports of adverse events involving medical devices. The database is searchable by the public and provides data files for downloading since 1991.
Vídeos
Ver tudo
www.accessdata.fda.gov › cfMAUDE › TextSearchMAUDE - Manufacturer and User Facility Device Experience

www.accessdata.fda.gov › cfMAUDE › TextSearch
- Em cache
30 de abr. de 2024 · The Manufacturer and User Facility Device Experience (MAUDE) database is a searchable database of medical device reports (MDRs) of adverse events involving medical devices over the last ten...
www.accessdata.fda.gov › cfMAUDE › SearchManufacturer and User Facility Device Experience (MAUDE) Database

www.accessdata.fda.gov › cfMAUDE › Search
- Em cache
30 de abr. de 2024 · The MAUDE database houses medical device reports submitted to the FDA by mandatory reporters 1 (manufacturers, importers and device user facilities) and voluntary reporters such as health care...
www.fda.gov › medical-devices › mandatory-reportingAbout Manufacturer and User Facility Device Experience (MAUDE)

www.fda.gov › medical-devices › mandatory-reporting
- Em cache
The FDA will continue to seek ways to improve the MAUDE database and the availability of MDR information. The MAUDE database : Contains the last ten years of MDR data.
open.fda.gov › data › maudeManufacturer and User Facility Device Experience

open.fda.gov › data › maude
- Em cache
MAUDE contains reports of suspected device-associated deaths, serious injuries and malfunctions submitted to the FDA by mandatory and voluntary reporters. Learn about the data sources, limitations, and how to access the database.
www.fda.gov › medical-devices › medical-deviceAdverse Event Reporting Data Files | FDA

www.fda.gov › medical-devices › medical-device
- Em cache
21 de jun. de 2019 · The FDA provides data files of adverse events involving medical devices reported by manufacturers, distributors, and user facilities. The data include MAUDE, DEN, and ASR data from 1984 to 2019.

Yahoo Search Busca da Web

Resultado da Busca

www.accessdata.fda.gov › cfdocs › cfmaudeManufacturer and User Facility Device Experience (MAUDE) Database

www.fda.gov › medical-devices › mandatory-reportingAbout Manufacturer and User Facility Device Experience (MAUDE)

Vídeos

www.accessdata.fda.gov › cfMAUDE › TextSearchMAUDE - Manufacturer and User Facility Device Experience

www.accessdata.fda.gov › cfMAUDE › SearchManufacturer and User Facility Device Experience (MAUDE) Database

www.fda.gov › medical-devices › mandatory-reportingAbout Manufacturer and User Facility Device Experience (MAUDE)

open.fda.gov › data › maudeManufacturer and User Facility Device Experience

www.fda.gov › medical-devices › medical-deviceAdverse Event Reporting Data Files | FDA

Buscas relacionadas