BEUDAMED
    13 results · 25ms · Sources: EU EUDAMED, US FDA

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    NEWTRON P5 XS B.LED

    FDA 510(k)
    FDA Class 2 ·Dental

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517637048·CoRoent Ant TLIF PEEK, 13x12x32mm 12°

    HHM

    FDA UDI
    Oticon A/S·05707131258786·H150, MINIRITE 312 WL SGR HHM

    Portex

    FDA UDI
    ICU MEDICAL, INC.·15019517071665·

    STINGRAY CERVICAL CAGE; SHARK IMPLANT (PLIF); BULL SHARK IMPLANT(PLIF); TIGER IMPLANT (TLIF); GREAT WHITE IMPLANTS(ALIF)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CLEAR-THERM MICRO HME, MODEL 1441

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    FENESTRATED BIPOLAR FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·April 9, 2014

    CD HORIZON BALLAST SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NKB·December 9, 2019

    ENERGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 1, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013

    RF MULTIGEN

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code GXD·June 11, 2011

    XVWEB

    FDA Adverse Event
    Injury ·PLANET DDS·Product code LLZ·March 13, 2025

    SECOND OPINION

    FDA Adverse Event
    Injury ·PEARL INC.·Product code MYN·March 13, 2025