BEUDAMED
    6 results · 17ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    VISION(R) LDH (LACTATE DEHYDROGENASE)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PREAMPLIFIER MODELS 8101PI & 8102PI

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    ArtiClip LAA Exclusion System

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

    LIGACLIP** MCA

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDO·October 25, 2010

    SCREW

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·December 20, 2012

    PEARL 8.0 HANDPIECE

    FDA Adverse Event
    Malfunction ·CARDIOGENESIS CORPORATION·Product code MNO·June 18, 2014