BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    CENTERING PLUG

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

    SOMATEX

    FDA UDI
    BIOPSYBELL SRL·08033860021658·

    RESPONSE 2000 HIP STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POWDER-FREE VINYL PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    TAXUS EXPRESS2 DRUG-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORP.·Product code NIQ·October 10, 2006

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR PURITAN BENNETT IRELAND·Product code CBK·May 6, 2014

    BIOGLUE SURGICAL ADHESIVE

    FDA Adverse Event
    Injury ·CRYOLIFE, INC.·Product code MUQ·January 7, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 26, 2010