BEUDAMED
    31 results · 23ms · Sources: EU EUDAMED, US FDA

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    CERVICAL CAGE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    K2M General Instruments

    FDA UDI
    VB Spine LLC·10888857554252·Parallel Trial Size 14x30x16 mm

    POWDER-FREE VINYL PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    POWDER FREE GREEN NEOPRENE SURGICAL GLOVES, STERILE WITH ALOE VERA

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    MONOSYN VIOLET 3/0 (2) 70CM HR26 (M) RCP

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAM·November 9, 2023

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·August 6, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·August 6, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·August 6, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·October 17, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·November 9, 2018

    ROSA ONE

    FDA Adverse Event
    Injury ·MEDTECH SA·Product code HAW·January 11, 2019

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code NAY·January 21, 2019

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·December 21, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code OLO·November 15, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code OLO·November 15, 2018

    SIG MOD TIB TRAY CEM COCR 2.5

    FDA Adverse Event
    Injury ·9616671 DEPUY (IRELAND)·Product code JWH·May 21, 2013

    ASCENDRA 3 INTRODUCER SHEATH SET

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code NPT·September 26, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 13, 2011

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code OLO·November 15, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·August 3, 2018