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

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    Yushan X-Ray Flat Panel Detector with DROC

    FDA 510(k)
    FDA Class 2 ·Radiology

    APEX PS Knee

    FDA UDI
    Omni Life Science, Inc.·00841690113287·PS Insert, Size 5 x 10mm

    SMARTLOCK

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·34546540355707·Locking Screws, Cross-Pin

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707022374·CALIBRA BANDS 2ND MOLAR n.SUR 10

    Zavation

    FDA UDI
    Zavation LLC·00842166132788·Ti3Z CIF 14mmx16mmx10mm -5 deg

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946059958·X SERIES, MONITOR/DEFIBRILLATOR, 3/5 LEAD, ECG,...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946010966·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946018689·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946071882·X SERIES, HOSPITAL, MONITOR/DEFIBRILLATOR, 3/5 ...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946014902·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...

    TRANSCEND

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

    SMOKE EVACUATION HOSES/TUBING

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

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946010973·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946059965·X SERIES, MONITOR/DEFIBRILLATOR, 3/5 LEAD, ECG,...

    X SERIES

    FDA UDI
    Zoll Medical Corporation·00847946017934·Defibrillator ,MAIN ASSY, X SERIES MONITOR/DEFI...

    ICY HOT HEAT THERAPY PATCH

    FDA Adverse Event
    Other ·CHATTEM, INC.·Product code IMD·October 27, 2008

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    POPULAR PLASTICS·Product code IKX·August 23, 2011

    OT VERIO PRO PLUS METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 11, 2013

    BINAXNOW COVID-19 AG SELF TEST 2CT

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·May 7, 2024

    BINAXNOW COVID-19 AG SELF TEST 2CT

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·May 7, 2024