BEUDAMED
    14 results · 22ms · Sources: EU EUDAMED, US FDA

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    PERFUSE PERCUTANEOUS DECOMPRESSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Biomet® Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304001428·

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172973868·

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172973783·

    FINISHING WIRE SUPPORTRAK

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VIPER F2 FACET FIXATION SYSTEM

    FDA 510(k)
    FDA Unclassified ·Unknown

    VANGAURD SSK INTERLOCKING FEMORAL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 4, 2014

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 28, 2013

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·June 27, 2011

    VANGUARD PS OPEN FEMORAL INTERLOCK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 18, 2017

    BIOMET OFFSET TIBIAL TRAY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 18, 2017

    VNGD SSK PSC TIB BRG 18X63/67

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·September 14, 2017

    VNGD SSK PSC INTLK FMRL 60 RT

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·July 21, 2016