BEUDAMED
    8 results · 24ms · Sources: EU EUDAMED, US FDA

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    KNEE PROSTHESIS DRIVER

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    DPI-1106 IMPLANT, MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Dental

    ALBUMIN REAGENT SET

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ZEPHYR XL DR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWP·January 15, 2014

    TRIDENT HEMI CUP

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code JDI·November 29, 2010

    LIFESHIELD PRIMARY PLUMSET, CLAVE, PORT CLAVE Y SITE

    FDA Adverse Event
    Malfunction ·HOSPIRA·Product code FPA·October 31, 2012

    BD BACTEC FX, INSTRUMENT TOP, PACKAGED

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MDB·February 22, 2021

    Exactech Equinoxe GLENOID,KEELED, CEMENTED, mates with 47, 50, 53 head, beta curvature, Sizes: a) Small, Item Number 314-02-02, b) Medium, Item Number 314-02-03, c) Large, Item Number 314-02-04, Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024