BEUDAMED
    12 results · 23ms · Sources: EU EUDAMED, US FDA

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    SHIMADZU IMAGE AMPLIFIER IA-12VSA SERIES

    FDA 510(k)
    FDA Class 2 ·Radiology

    Class A Outdoor 21 - 16 Poly White

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588620121·Class A Outdoor 21 - 16 Poly White

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707059837·DB BRACKETS 12 EXTREMO NO-Ni 22 T+8 A+9

    Color Cuff

    FDA UDI
    STRYKER CORPORATION·07613154599813·Non-Sterile Reusable Tourniquet Cuff Single Bla...

    Color Cuff

    FDA UDI
    STRYKER CORPORATION·07613154599837·Non-Sterile Reusable Tourniquet Cuff Single Bla...

    Z-MED Z-MED II

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SYNTHES LOW PROFILE NEURO SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    THERMAL SENSORY ANALYZER (TSA-II)

    FDA Adverse Event
    Injury ·MEDOC LTD., ADVANCED MEDICAL SURGERY MEDISCENSE USA·Product code LQW·December 26, 2019

    HUT EXT DR FINAL ASSY-STANDARD

    FDA Adverse Event
    Malfunction ·LIEBEL-FLARSHEIM CO.·Product code IXR·January 15, 2013

    LIGASURE ATLAS HANDSWITCHING 37CM

    FDA Adverse Event
    Malfunction ·COVIDIEN LLC (SHANGHAI)·Product code GEI·December 8, 2010

    ENERGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 9, 2014

    QSENSE CPM THERMAL SENSORY ANALYZER 2001

    FDA Adverse Event
    Malfunction ·MEDOC LTD, ADVANCED MEDICAL SYSTEM·Product code LQW·April 19, 2022