BEUDAMED
    12 results · 36ms · Sources: EU EUDAMED, US FDA

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    Ezfil

    FDA 510(k)
    FDA Class 2 ·Dental

    Bernafon

    FDA UDI
    Bernafon AG·05711584087114·ZR3, KIT 10 85 PB BE ZERENA 3

    HYDRUS MICROSTENT

    FDA Adverse Event
    Injury ·IVANTIS INC·Product code OGO·February 12, 2026

    WEBSTER DUO-DECAPOLAR CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EASY RA D BIL REAGENT MODEL 10212, EASY RA GLU-H REAGENT MODEL 10200

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CD SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Injury ·SOFAMOR DANEK EUROPE·Product code KWQ·December 8, 1999

    COCHLEAR OSIA OSI300 IMPLANT

    FDA Adverse Event
    Injury ·COCHLEAR LTD·Product code PFO·March 8, 2026

    MEDIUM BEALL VALVE

    FDA Adverse Event
    Death ·UNKNOWN·Product code DYE·May 13, 1992

    TENDRIL STS

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, CRMD·Product code DTB·January 13, 2014

    ARCTIC FRONT CARDIAC CRYOABLATION CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code OAE·August 4, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 27, 2013

    AIR DERMATOME HANDPIECE

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code GFD·February 5, 2014