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

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    PROTECTIVE RESTRAINT (VEST RESTRAINT)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ZERO PROFILE ANTERIOR CERVICAL PLATE (ACP) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Prontosan Wound Gel

    FDA 510(k)
    FDA Unclassified ·Unknown

    SYMPHONY BREAST PUMP

    FDA Adverse Event
    Injury ·MEDELA A G·Product code HGX·February 13, 2013

    ROBOTIC SURGERY

    FDA Adverse Event
    Injury ·Product code NAY·July 24, 2014

    UNKNOWN DEPUY POLY DIAL LINER 10 DEG + 328MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWA·January 17, 2011

    FREEDOM 10 DEG LINER SZ 24

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWZ·November 25, 2014

    ACT ARTIC HD ARCOM XL 28X50MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWZ·December 15, 2014

    M2A-MAGNUM PF CUP 56ODX50ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·December 15, 2014

    FREEDOM CONSTRAINED HEAD-6MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWZ·December 15, 2014

    XP-XP Tibial Tray - Interlok 63 mm Item # 195751

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·September 18, 2019