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

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    Filters Regulation: Us FDA ×

    AESCULAP CRANIOFIX TITANIUM CLAMP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295250999·SIGMA CURVED PLUS INSERT TRIAL SIZE 2 12.5mm

    MONITOR, CARDIAC, BEDSIDE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VARI-LASE WIRE FIBER

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

    FOLEY CATHETER, 2W SEC STD CH14

    FDA Adverse Event
    Malfunction ·UNOMEDICAL SDN BHD·Product code KOD·February 15, 2013

    RENAISSANCE 26 STRETCHER 11/00

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MED DIV·Product code FPO·December 30, 2010

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·July 31, 2014

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·September 18, 2024