BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Signia Circular Adapters (for use with Signia Staplers), Tri-Staple 2.0 Circular Reloads (for use with Signia Circular Adapters)

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

    XTRACT SYRINGE KEY SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    REVEAL XT INSERTABLE CARDIAC MONITOR, MODEL 9529, REVEL DX INSERTABLE CARDIAC MONITOR, MODEL 9528

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    REVERSE SHOULDER SYSTEM THREADED GLENOID BASEPLATE Ø27X35

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·May 13, 2020

    REVERSE SHOULDER SYSTEM GLENOID BASEPLATE Ø27X15

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·November 20, 2019

    REVERSE SHOULDER SYSTEM GLENOID BASEPLATE Ø27X25

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·November 14, 2019

    SIMILE

    FDA Adverse Event
    Injury ·PENTRON CLINICAL·Product code EBF·June 21, 2013

    SCORPIO NRG X3 PS TIBIAL INSERT #7 12MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·July 19, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·October 17, 2014

    REVERSE SHOULDER SYSTEM GLENOID POLYAXIAL LOCKING SCREW - L30

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code PHX·June 19, 2019