Yahoo Search Busca da Web

Resultado da Busca

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

   www.accessdata.fda.gov › cfdocs › cfmaude

   • Em cache

   31 de mai. de 2024 · The MAUDE database contains adverse event reports of medical devices submitted to the FDA by mandatory and voluntary reporters. Users can search the database by simple or advanced options, or download MDR files from the FDA website.

   • 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)...

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

   www.accessdata.fda.gov › cfMAUDE › Search

   • Em cache

   31 de mai. 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...

3. Imagens

   • 
   • 
   • 

   Ver tudo

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

   www.accessdata.fda.gov › cfMAUDE › TextSearch

   • Em cache

   31 de mai. 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...

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

   www.fda.gov › medical-devices › mandatory-reporting

   • Em cache

   The MAUDE database contains adverse event reports of medical devices submitted by manufacturers, importers, and user facilities. Learn about the database description, limitations, fields, and how to access the data files and disclaimers.

6. 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 by manufacturers, importers, device user facilities and others. The FDA uses MAUDE to monitor device performance, detect safety issues and contribute to benefit-risk assessments.

7. www.fda.gov › medical-devices › medical-device-safetyMedical Device Reporting (MDR): How to Report Medical Device ...

   www.fda.gov › medical-devices › medical-device-safety

   • Em cache

   27 de jul. de 2023 · The Manufacturer and User Facility Device Experience (MAUDE) database contains mandatory reports filed by manufacturers and importers from August 1996 to present, all mandatory user...

8. www.ncbi.nlm.nih.gov › books › NBK570582Use and Application Of MAUDE In Patient Safety - StatPearls ...

   www.ncbi.nlm.nih.gov › books › NBK570582

   24 de abr. de 2023 · The Manufacturer and User Facility Device Experience (MAUDE) database is an online searchable and publicly accessible repository developed by the United States Food and Drug Administration (FDA) for systematic data collection of adverse outcomes related to the medical devices.