BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

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    TOTAL HIP, CHARNELY TYPE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Lacrimal Dilator

    FDA UDI
    KATENA PRODUCTS, INC.·00841668108642·WILDER LACRIMAL DILATOR #2

    Performa®

    FDA UDI
    Merit Medical Systems, Inc.·00884450005118·

    PARAMOUNT INTERVERTEBRAL BODY FUSION DEVICE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Veress Needle

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    COBALT CHROME +5 HUMERAL TRAY

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code KWS·September 5, 2017

    E1 44-36 STD +3 HMRL BRG

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code PAO·March 8, 2018

    DUROM ACETABULAR COMPONENT

    FDA Adverse Event
    Other ·ZIMMER GMBH·Product code KWA·April 9, 2014

    FREESTYLE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code NBW·June 27, 2007

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 2, 2012

    RINGLOC REPLACEMENT HUMERAL TRAY RING

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code LPH·September 5, 2017