BEUDAMED
    12 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    EFAI RTSuite CT HN-Segmentation System

    FDA 510(k)
    FDA Class 2 ·Radiology

    KONAN SPECULAR MICROSCOPE XIV

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    REPICCI II UNICONDYLAR KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·July 16, 2021

    ARTHREX®

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HRX·May 13, 2019

    ARTHREX®

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HRX·May 13, 2019

    ARTHREX®

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HRX·May 13, 2019

    LINEAR? ST

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·September 15, 2025

    CONCERTO

    FDA Adverse Event
    Malfunction ·ARJO HOSPITAL EQUIPMENT AB·Product code FPO·October 31, 2008

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·August 23, 2011

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·July 11, 2013

    CWIII ARTHROSCOPY PUMP

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRX·June 19, 2019