BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    HUMAN C1 INACTIVATOR OR C-1 ESTERASE INHIBITOR RADIAL IMMUNODIFFUSION KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    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

    Centros Long-Term Hemodialysis Catheter, CentrosFLO Long-Term Hemodialysis Catheter

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

    REVOLUTION XR/D DIGITAL RADIOGRAPHIC IMAGING SYSTEM WITH TOMOSYNTHESIS

    FDA 510(k)
    FDA Class 2 ·Radiology

    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

    CAPSURE Z NOVUS

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·February 9, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·January 7, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 23, 2014