BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    UNI-LASER 430

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    HYCOR SENTRY(TM) DRUGS OF ABUSE URINE CALIBRATORS

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    LIGHT DIAGNOSTICS HUMAN METAPNEUMOVIRUS DFA KIT, MODEL CATALOG NUMBER 3124

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ARTICULEZE M HEAD 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·July 30, 2013

    PINNACLE MTL INS NEUT36IDX58OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·July 30, 2013

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·February 19, 2016

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDIC, INC.·Product code KWP·April 9, 2015

    PARADIGM INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 11, 2015

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·January 13, 2011

    ATTAIN ABILITY

    FDA Adverse Event
    Injury ·MPRI·Product code OJX·August 8, 2014

    DCP 4.5-BROAD 11HO L183 SST

    FDA Adverse Event
    Injury ·SYNTHES GRENCHEN·Product code HRS·February 23, 2017