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

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    Ziehm Vision RFD 3D

    FDA 510(k)
    FDA Class 2 ·Radiology

    ID NOW COVID 19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·June 2, 2021

    RADIFOCUS GLIDEWIRE M

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·January 22, 2018

    NUCLISENS EASYQ MRSA; NUCLISENS EASYQ ANALYZER; NUCLISENS EASYQ INCUBATOR (110 VOLT); NUCLISENS DIRECTOR V.2.6

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ISC-1000 PENTAX CONFOCAL LASER SYSTEM

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

    LEOPARD IMPLT 5DEG, LRDTC,28X7

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES SPINE·Product code MQP·June 3, 2013

    ASR UNI FEMORAL IMPL SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KXA·June 23, 2011

    PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code NIQ·August 27, 2008

    VARIABLE SELF-DRILLING SCREW DIAM. 4X14MM (2X)

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWQ·October 4, 2017