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

   www.accessdata.fda.gov › cfdocs › cfmaude

   • En caché

   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...

   • Standards

     Medical Device Reports (MAUDE) CDRH Export Certificate...

   • CLIA

     Aquí nos gustaría mostrarte una descripción, pero el sitio...

   • Adverse Events

     The Manufacturer and User Facility Device Experience (MAUDE)...

   • Download Files

     The FDA uploads these into the MAUDE database and includes...

   • MDR Data Files Webpage

     Like all MDR data in MAUDE, MDR data in ASR reports cannot...

   • Cdrh FOIA Electronic Reading Room

     Aquí nos gustaría mostrarte una descripción, pero el sitio...

   • FDA Guidance Documents

     Some FDA guidance documents on this list are indicated as...

   • Post-Approval Studies

     Mandated Studies Program Food and Drug Administration 10903...

2. getmaude.com › collections › all-productsSelf Care Products | Personal Care Products – maude

   getmaude.com › collections › all-products

   • En caché

   We created fairly-priced, bath and bedroom essentials for all people. Shop now for maude personal wellness products like natural condoms, lubricants and more.

3. maudestudio.comExpertos en Formación oficial, programada y privada | Maude ...

   maudestudio.com

   • En caché

   Maude Studio, expertos en formación. 40 años de experiencia impartiendo cursos subvecionados, formación programada para empresas y formación privada. Acceso al campus Acceso colaborador 952 225 571 info@maudestudio.com

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

   www.accessdata.fda.gov › cfMAUDE › Search

   • En caché

   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 years. Reports older than ten years are provided on the FDA's MDR Data Files webpage.

5. maudestudio.com › login › teleformacionAcceso - Maude Studio

   maudestudio.com › login › teleformacion

   Acceso Teleformación. Complete el formulario inferior para acceder al servicio.

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

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

   • En caché

   23 de oct. de 2023 · Linkedin. Manufacturer and User Facility Device Experience (MAUDE) database represents reports of adverse events involving medical devices. The searchable database contains the last 10 years of...

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

   open.fda.gov › data › maude

   • En caché

   About . MAUDE Each year, the FDA receives several hundred thousand medical device reports (MDRs) of suspected device-associated deaths, serious injuries and malfunctions. The FDA uses MDRs to monitor device performance, detect potential device-related safety issues, and contribute to benefit-risk assessments of these products.