BEUDAMED
    9 results · 26ms · Sources: EU EUDAMED, US FDA

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    TWO-CHANNEL PREAMPLIFIER

    FDA 510(k)
    FDA Class 2 ·Neurology

    INFUSOR SMALL VOLUME ELASTOMERIC INFUSION DEVICES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Rocket Indwelling Peritoneal Catheter (IPC) Insertion Kit

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

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·August 16, 2017

    XENIUM XPM

    FDA Adverse Event
    Malfunction ·NIPRO CORPORATION *USD*·Product code KDI·February 14, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 29, 2014

    ASR ACETABULAR CUPS 54

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD.·Product code KWA·January 7, 2011

    PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·October 15, 2025

    GII OVAL RESURFACING PAT 32MM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·December 18, 2015