BEUDAMED
    9 results · 43ms · Sources: EU EUDAMED, US FDA

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    RIFTON MOR219 19 & RIFTON MOR225 25

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    Bosworth Superbite

    FDA UDI
    Harry J Bosworth Company·H66809218171·ZOE Bite Regist. Paste Catalyst

    VCARE A

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

    AARON A950 HIGH FREQUENCY ELECTROSURGICAL GENERATOR, AARON A950 ELECTROSURGICAL GENERATOR, 240V

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

    TARGETING ARM T2 PROX. HUM.

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·June 27, 2012

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 29, 2014

    EON

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 14, 2013

    PUMP MMT-522LNAS PRDGM INS SK EN ML

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·December 6, 2010

    GXL acetabular liners, orthopedic hip implant component. Product Line Numbers: a. GXL NEUTRAL LINER, G0 28MM ID, 130-28-50; b. GXL NEUTRAL LINER, G00 22MM ID, 130-22-70; c. NOVATION GXL LIPPED LINER, G0 28MM ID, 132-28-50; d. NOVATION GXL LIPPED LINER, G00 22MM ID, 132-22-70;

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·September 21, 2022