BEUDAMED
    74 results · 25ms · 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 ×

    Baha 5 Power Sound Processor

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    OSS™ Orthopedic Salvage System

    FDA UDI
    Biomet Orthopedics, LLC·00880304554733·

    QUEST

    FDA UDI
    Asp Global, LLC·00840216116313·6” X 9” 1.5MIL, EMPLOYER SOLUTIONS, W/3” FOLD O...

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916141929·ZEUS®-L Rasp, Scraper

    QUEST

    FDA UDI
    Asp Global, LLC·00840216120075·EMPLOYER SOLUTIONS-ADHESIVE BAG

    QUEST

    FDA UDI
    Asp Global, LLC·00840216120013·EMPLOYER SOLUTIONS-ADHESIVE BAG

    QUEST

    FDA UDI
    Asp Global, LLC·00840216120020·EMPLOYER SOLUTIONS-ADHESIVE BAG

    Sentry Lateral Plating System

    FDA UDI
    Life Spine, Inc.·00190837030254·SENTRY 2 Set Screw

    PALM ECG RECORDER, MODEL EP-201/202

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NEXFIN MODEL 2

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD VACUTAINER® K2E 3.6MG PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 6, 2019

    BD VACUTAINER® K2E 3.6MG PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 6, 2019

    INDIGO SYSTEM ASPIRATION CATHETER D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·February 12, 2019

    INDIGO SYSTEM SEPARATOR D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·April 18, 2018

    INDIGO SYSTEM CATD ASPIRATION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·May 29, 2019

    INDIGO SYSTEM CATD ASPIRATION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·January 17, 2020

    BD VACUTAINER® K3E 7.2MG PLUS BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code PJE·May 1, 2018

    INDIGO SYSTEM ASPIRATION CATHETER D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·December 7, 2018

    INDIGO SYSTEM ASPIRATION CATHETER D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code QEW·January 29, 2021

    INDIGO SYSTEM ASPIRATION CATHETER D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·December 10, 2020