BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    Dawn Diode Laser System

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

    TURBO-JECT PERIPHERALLY INSERTED CENTRAL VENOUS CATHETER (PICC) SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    VIDAPORT INTRAOSSEOUS INFUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TURBO-JECT® DOUBLE LUMEN POWER-INJECTABLE PICC

    FDA Adverse Event
    Injury ·COOK INC·Product code LJS·December 3, 2015

    BD PERISAFE¿ EPIDURAL ANAESTHESIA KITS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL DEVICES CO., LTD. SUZHOU·Product code CAZ·February 3, 2022

    GO BED PLUS

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·July 19, 2011

    TSH, THYROTROPIN

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JLW·November 6, 2014

    PROMUS ELEMENT? PLUS

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·July 18, 2013