BEUDAMED
    8 results · 33ms · Sources: EU EUDAMED, US FDA

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    DAY SUN INDUSTRIAL CORP

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    1.8 MM PHOENIX ATHERECTOMY CATHETER, 2.2 MM PHOENIX ATHERECTOMY CATHETER, PHOENIX HANDLE, PHOENIX WIRE SUPPORT CLIP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RESCONTROL II

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    KAPPA 400 DR

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·August 9, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DTB·August 9, 2013

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·January 16, 2013

    ASR ACETABULAR IMPLANT 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·December 17, 2010

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 17, 2014