BEUDAMED
    366 results · 22ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    SALINE/ CONTRAST MEDIA INFUSION CATHETER

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    HENKE SASS WOLF SAPHENOUS VEIN LAPAROSCOPE

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

    PAIN CARE MULTI-PORT CATHETER, MODEL 2000L

    FDA 510(k)
    FDA Class 2 ·General Hospital

    0009613348-2023-063611

    FDA Adverse Event
    Injury ·INSTITUT STRAUMANN AG·Product code DZE·June 16, 2023

    FLIPPER 110 PDA CLOSURE COIL DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·WILLIAM COOK EUROPE·Product code KRD·January 2, 2017

    HUDSON ENDOTRACHEAL TUBE, HVT, 7.5

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code BTR·April 12, 2013

    AXSYM RUBELLA IGG ANTIBODY

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code LFX·June 19, 2008

    PK7312-03 AUTOMATED MICROPLATE SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER MISHIMAK.K.·Product code KSZ·April 19, 2011

    NMIC-312

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 16, 2026

    MREYE FLIPPER PDA CLOSURE DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·WILLIAM COOK EUROPE·Product code KRD·June 13, 2018

    PANEL PHOENIX NMIC-312

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

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026

    BD PHOENIX¿ NMIC/ID-307

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

    BD PHOENIX¿ NMIC/ID-307

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

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    FLIPPER 110 PDA CLOSURE COIL DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·WILLIAM COOK EUROPE·Product code KRD·March 8, 2017

    MREYE FLIPPER PDA CLOSURE DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·WILLIAM COOK EUROPE·Product code KRD·March 8, 2017

    BD PHOENIX¿ NMIC/ID-307

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

    BD PHOENIX¿ NMIC/ID-307

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