BEUDAMED
    11 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 ×

    ACOUSTASCOPE ESOPHAGEAL STETHOSCOPE W/TEMP SENSOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994806796·LID 1854212 DEGEN TAG SORTER LID

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209127634·

    Shoreline ACS

    FDA UDI
    Seaspine Orthopedics Corporation·10889981125424·4.0mm Variable Screw, Self Drilling, 12mm

    Colored Chain

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746058134·CHAIN PLASTIC 15' LONG CLEAR

    Colored Chain

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746032691·CHAIN PLASTIC 15' LONG CLEAR

    STIMTECH SD CLINICIAN 6090 #78-8055

    FDA 510(k)
    FDA Class 2 ·Neurology

    N-CHANNEL

    FDA 510(k)

    ARTICULEZE M HEAD 36MM +5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·June 6, 2014

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·December 3, 2012

    TERUMO VIRTUOSAPH VEIN HARESTING SYSTEM

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code GCJ·September 3, 2010