BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    CX50 Diagnostic Ultrasound System, Sparq Diagnostic Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    K162309

    FDA Adverse Event
    Malfunction ·MEDTRONIC NAVIGATION, INC·Product code PGW·November 14, 2019

    OMNI PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NANOKNIFE SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    LINER: VERSAFITCUP DM DOUBLE MOBILITY HC LINER Ø 60/28

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·December 20, 2019

    CALYPSO

    FDA Adverse Event
    Malfunction ·ARJO HOSPITAL EQUIPMENT AB·Product code FSA·May 10, 2013

    PFC SIGMA STAB INS SZ2 8MM

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM, A DIVISION OF DEPUY ORTHOPAEDICS, INC.·Product code JWH·July 7, 2011

    POWERVAR 230V POWERSUPPLY

    FDA Adverse Event
    Malfunction ·DRAEGER MEDICAL SYSTEMS, INC (IT/M)·Product code BSZ·September 8, 2008