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

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    Niti-S Esophageal Stent; Esophageal TTS Stent

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

    Fogarty Corkscrew Catheters; Fogarty Graft Thrombectomy Catheters

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    e-SDF

    FDA 510(k)
    FDA Class 2 ·Dental

    BD VACUTAINER® MULTIPLE SAMPLE LUER ADAPTER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·November 6, 2025

    BD VACUTAINER® MULTIPLE SAMPLE LUER ADAPTER

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·November 19, 2025

    LIFEPAK 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·July 27, 2011

    SPECTRANETICS GLIDELIGHT LASER SHEATH

    FDA Adverse Event
    Injury ·SPECTRANETICS CORPORATION·Product code MFA·November 11, 2014

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·July 23, 2013

    G7 E1 LINER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·June 14, 2018

    G7 SHELL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·June 14, 2018

    G7 HI-WALL E1 LINER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·June 14, 2018