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

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    PASS LP SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Bernafon

    FDA UDI
    Bernafon AG·05711584050965·CA3 ITED, WL L BE CARISTA 3

    FIRST SIGN DRUG OF ABUSE SCREENING TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    ORTHO MTA (MINERAL TRIOXIDE AGGREGATE)

    FDA 510(k)
    FDA Class 2 ·Dental

    GENISTRONG

    FDA Adverse Event
    Malfunction ·GENICON·Product code GCJ·October 15, 2017

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·August 5, 2019

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·September 6, 2019

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·February 5, 2019

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·May 29, 2013

    SYNCHROMED

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·October 1, 2014

    PROTÉGÉ ®GPS¿ SELF EXPANDING NITINOL STENT

    FDA Adverse Event
    Injury ·EV3 INC.·Product code FGE·June 17, 2011

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·July 7, 2025