BEUDAMED
    282 results · 25ms · Sources: EU EUDAMED, US FDA

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    GALT MEDICAL GUIDEWIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SUPER C HEMODIALYSIS/APHERESIS CHRONIC CATHETER, MODEL DC-36 SERIES, DC-40 SERIES, DC-45 SERIES

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

    COMPAT REPLACEMENT GASTROSTOMY TUBE KIT, MODEL 0974XX

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

    ASR ACETABULAR CUPS 50

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·April 3, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Other ·INVACARE·Product code CAW·March 22, 2011

    BAK/C CERVICAL INTERBODY

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE, INC·Product code LXH·April 16, 2008

    MARKERS

    FDA Adverse Event
    Malfunction ·PRAXIM·Product code HAW·January 3, 2007

    BD PHOENIX¿ NMIC-311

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 19, 2026

    BD PHOENIX¿ NMIC-311

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 19, 2026

    BD PHOENIX¿ NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 28, 2026

    BD PHOENIX¿ NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 14, 2026

    BD PHOENIX¿ NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 3, 2026

    BD PHOENIX¿ NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code LON·May 27, 2026

    BD PHOENIX¿ NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 20, 2026

    BD PANEL PHOENIX NMIC-311

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·August 18, 2024

    MONOPLUS VIOLET 0 (3,5) 90CM HR37S(M)RCP

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.U.·Product code NEW·December 14, 2021

    BD PHOENIX¿ NMIC-306

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 1, 2026

    MONOPLUS C VIOLET 2/0 (3) 25M

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code NEW·January 2, 2019

    MONOPLUS VIOLET 4/0 (1.5) 70CM HR17 (M)

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code NEW·October 23, 2019