BEUDAMED
    11 results · 22ms · Sources: EU EUDAMED, US FDA

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    ALTRATOUCH 1000 HEMODIALYSIS DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    LGN PS HIGH FLEX XLPE SZ 1-2 13MM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·August 9, 2017

    GII PS HI FLEX ISRT SZ 7-8 9

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·July 19, 2017

    VIBRONICS AUTO CORE BIOPSY DEVICE (ACBD)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    INTRA-ARTICULATED ARTHROSCOPIC POWER SYSTEM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    LGN PS HIGH FLEX XLPE SZ 1-2 13MM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·August 9, 2017

    GII ARTICULAR INSERTER/EXTRACT

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBH·February 9, 2018

    UNKNOWN_RECONSTRUCTIVE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·February 11, 2013

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011

    ALLIGATOR RETRIEVAL DEVICE

    FDA Adverse Event
    Injury ·EV3 NEUROVASCULAR·Product code DQY·July 24, 2014

    BD BACTEC PEDS PLUS/ F CULTURE VIALS

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MDB·July 14, 2021