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

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    PRECISION BIPOLAR COAGULATOR

    FDA 510(k)
    FDA Class 2 ·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 PS HI FLEX ISRT SZ 7-8 9

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

    BIOVALVE MINI-JECT NEEDLEFREE INJECTOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PowerPICC® EtOH Catheter and PowerPICC SOLO®2 EtOH Catheter

    FDA 510(k)
    FDA Class 2 ·General Hospital

    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

    CAPSUREFIX NOVUS MRI

    FDA Adverse Event
    Injury ·MPRI·Product code NVN·February 9, 2013

    TRI-LOCK BPS SZ9 HI OFFSET

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.1818910·Product code KWA·July 23, 2014

    ACTIVA PC

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·January 4, 2011