BEUDAMED
    71 results · 21ms · 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 ×

    Upper Arm Blood Pressure Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TLS 5.0

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030CK2212120·Enhanced Graft Interbody Cage 7DEG x 22L x 12W ...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946061593·X SERIES ADVANCED, MONITOR/DEFIBRILLATOR, 12 LE...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946097776·X SERIES ADVANCED, MONITOR/DEFIBRILLATOR, 12 LE...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946029647·X SERIES ADVANCED, 12 LEAD W/INTERP, PACE, SPO2...

    ZAVATION CONNECTOR

    FDA UDI
    Zavation LLC·00197157021177·Open-Open/Small-Xsmall 12mm Offset Connector

    Voyant Open Fusion Device

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

    24CM POURCHEZ XPRESSO TWIN LUMEN CHRONIC HEMODIALYSIS CATHETER WITH SEPARATED TIPS

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

    Chord-X Premeasured Loops and Suture System

    FDA UDI
    ON-X LIFE TECHNOLOGIES, INC.·00813570020114·Artificial chordal replacement prosthesis

    Chord-X Premeasured Loops and Suture System

    FDA UDI
    ON-X LIFE TECHNOLOGIES, INC.·00813570020015·Artificial chordal replacement prosthesis

    BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·December 8, 2023

    BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·December 8, 2023

    PINNACLE PELVIC FLOOR REPAIR KIT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FTM·November 5, 2008

    ABBOTT AXSYM SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·August 24, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·July 11, 2013

    BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code FPA·December 1, 2023

    BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Injury ·BECTON, DICKINSON AND COMPANY (BD)·Product code FPA·February 16, 2024

    BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FPA·November 14, 2023

    BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Injury ·BECTON, DICKINSON & CO., (BD)·Product code FPA·December 28, 2023

    BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FPA·March 18, 2024