BEUDAMED
    12 results · 27ms · Sources: EU EUDAMED, US FDA

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    XTREL, MODEL NUMBER 3425

    FDA 510(k)
    FDA Class 2 ·Neurology

    SUPERELELASTIC NITINOL PISTON, SUPERELASTIC NITINOL TRIMMABLE PISTON, MODEL SPL03.39/40/41/42 (DETAILS IN 510(K) ANNEX 2

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    RESPITRACE 300SC

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 9, 2024

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 9, 2024

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 9, 2024

    ALARIS PCA MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION CORPORATION·Product code FRN·February 12, 2014

    ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE SYSTEM

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code NTE·October 27, 2010

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION·Product code DRM·November 15, 2012

    VGXP XP E1 TIB BRG RL 12X71

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·February 12, 2018

    VNGD XP INLK PRI TIB TRAY 73MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·February 12, 2018

    VGXP INTLK FMRL RT 60

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·February 12, 2018