BEUDAMED
    14 results · 24ms · Sources: EU EUDAMED, US FDA

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    AMERIMED ULTRASONIC SURGICAL ASPIRATION KIT

    FDA 510(k)
    FDA Unclassified ·Unknown

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867047327·LO-PRO SCRW TM,SS 3.5X 22MMCORT

    AUTOMATED BLOOD PRESSURE SPHYGMOMANOMTR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SONY UP-DF750 DIGITAL FILM IMAGER

    FDA 510(k)
    FDA Class 2 ·Radiology

    GRANUFLO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 9, 2014

    ENDOPATH ETS FLEX45

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GDW·October 4, 2010

    X-STREAM

    FDA Adverse Event
    Malfunction ·DAVOL INC., SUB. C.R. BARD, INC.·Product code GCJ·November 15, 2012

    CLAV FRAC PLT,CENTRAL THIRD,RT,SS

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRS·June 25, 2019

    ANTEROLAT DIST TIB PLT, SS, RIGHT, 16H

    FDA Adverse Event
    Injury ·ARTHREX INC.·Product code HRS·June 14, 2018

    LO-PRO LOCK SCRW,SS 2.7X 14MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·March 13, 2019

    LO-PRO SCRW TM,SS 3.5X 12MMCORT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·March 13, 2019

    LO-PRO SCRW TM,SS 3.5X 22MMCORT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·March 13, 2019

    LOCK DISTAL FIBULA PLT,SS RT,6H

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRS·March 13, 2019

    LO-PRO LOCK SCRW,SS 2.7X 12MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·March 13, 2019