BEUDAMED
    13 results · 17ms · Sources: EU EUDAMED, US FDA

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    VIDEO CAMERA W/ ELECTRONIC SHUTTER MODEL VCE-10

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Clinical review 2MP

    FDA UDI
    Barco NV·05415334000490·MDRC-2321 SNIB

    JOSTENT SELFX, MODELS 015SX4406; 015SX4408; 015SX4410; 015SX680; 015SX6808; 015SX6810

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

    BIOPLEX 2200 CELIAC IGA AND IGG KITS ON THE BIOPLEX 2200 SYSTEM, BIOPLEX 2200 CELIAC IGA AND IGG CALIBRATOR SETS, AND BI

    FDA 510(k)
    FDA Class 2 ·Immunology

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·January 25, 2013

    MED-EL COMBI 40+ COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·MED-EL ELEKTROMEDIZINISCHE GERAETE, GMBH·Product code MCM·March 10, 2014

    STENOSCOPE

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD·Product code JAA·December 2, 2010

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·September 12, 2016

    UNKNOWN KNEE TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·April 15, 2020

    UNKNOWN KNEE FEMORAL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·April 15, 2020

    PFC*SIGMA/RD/DOME PAT 3PEG,35

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·April 15, 2020

    SIG MOD TIB TRAY CEM COCR 2.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·April 15, 2020

    DEPUY SYNTHES (JOHNSON AND JOHNSON) GLOBAL ADVANTAGE COCR HUMERAL HEAD

    FDA Adverse Event
    Injury ·DEPUY SYNTHES/JOHNSON AND JOHNSON MEDICAL·Product code KWS·February 28, 2020