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

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    Filters Regulation: Us FDA ×

    OSTEONICS ALL POLYETHYLENE GLENOID SHOULDER COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Sierra

    FDA UDI
    Seaspine Orthopedics Corporation·10889981095680·Locking Cap Caddy

    EMBRYO TRANSFER CATHETER WITH ACCESSORY STYLET, MODELS 9018, 9023, 9018-S, 9023-S

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Interbody Fusion (IBF)/Vertebral Body Replacement(VBR) System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LOCKING TITANIUM ADAPTER

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·February 8, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·January 6, 2011

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·July 11, 2014

    MENTOR MEMORYGEL XTRA BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·March 19, 2024

    MENTOR MEMORYGEL XTRA BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·January 11, 2024