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

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    Filters Regulation: Us FDA ×

    SOVEREIGN™ Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BLUNT FILL NEEDLE AND BLUNT PLASTIC CANNULA

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MEDTRADE PRODUCTS CELOX SOLBAG, ANTI - COAGULANT

    FDA 510(k)
    FDA Unclassified ·Unknown

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·April 4, 2018

    PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code NEW·April 4, 2018

    OSTAPEK VBR CAGE

    FDA Adverse Event
    Injury ·COLIGNE AG·Product code MQP·September 19, 2019

    CD HORIZON BALLAST SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NKB·December 9, 2019

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 17, 2013

    ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE SYSTEM

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code NTE·April 30, 2008

    BONE SCREWS, CROSS-PIN, SELF-TAPPING, DIAM. 1.2X6MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS FREIBURG·Product code JEY·June 23, 2011