BEUDAMED
    11 results · 23ms · Sources: EU EUDAMED, US FDA

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    SHAW SUN SYSTEMS 1000, 2000 & 3200

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

    RECLAIM

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295533788·RECLAIM MONOBLOC REVISION FEMORAL STEM STANDARD...

    FIXATION STAPLE KIT - DLIDE HAMMER

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    VIOLET RED BILE AGAR

    FDA 510(k)
    FDA Class 1 ·Microbiology

    HIP GENERAL OFFSET-30° BROACH HANDLE - RIGHT

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LXH·April 3, 2019

    HIP GENERAL OFFSET-30° BROACH HANDLE - RIGHT

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LXH·May 17, 2019

    HIP GENERAL OFFSET-30° BROACH HANDLE - RIGHT

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LXH·March 21, 2019

    HIP GENERAL OFFSET-30° BROACH HANDLE - RIGHT

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LXH·July 26, 2019

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·June 6, 2014

    ORTHOPAT PERIOPERATIVE AUTOTRANSFUSION SYSTEM

    FDA Adverse Event
    Malfunction ·HAEMONETICS CORP.·Product code CAC·November 29, 2012

    HEARTSTART XL

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·September 30, 2010