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

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    PEP (POSITIVE EXPIRATORY PRESSURE) THERAPY DEVICE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Titan™

    FDA UDI
    Ascension Orthopedics, Inc.·10381780467779·RSS Double Drill Guide-S

    Titan Reverse Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556863589·RSS DOUBLE DRILL GUIDE-S

    RnD TE and RnD SE

    FDA 510(k)
    FDA Class 2 ·Dental

    TREND ANALYZER

    FDA 510(k)
    FDA Class 1 ·Cardiovascular

    SMARTSET GHV GENTAMICIN 40G

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LOD·December 12, 2017

    KIT 11.5FX19.5CM MAHURRKAR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code LFJ·January 17, 2013

    PROGRASP FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 28, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·January 12, 2011

    VALVE CONDUIT CONTEGRA

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code MWH·June 27, 2014