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

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    PORT-A-POLE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PRESTIGE® Cervical Disc System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00721902723254·DISC 6961470 PRESTIGE ARTIFICIAL 7X14MM

    P.F.C. SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295238973·P.F.C. SIGMA STABILIZED TIBIAL INSERT TRIAL SZ ...

    Internal Distraction - Sterile

    FDA 510(k)
    FDA Class 2 ·Dental

    DEL SOL BLUE LIGHT THERAPY SYSTEM

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

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·January 3, 2024

    PRESTIGE CERVICAL DISC SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC INC.·Product code MJO·February 5, 2010

    IN TOUCH ZU

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·January 17, 2013

    HEARTSTART XL

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·January 9, 2011

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·July 28, 2014

    INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code MAV·February 27, 2024

    INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code MAV·March 21, 2024