BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    AFP SYSTEM PULSE GENERATOR MODEL 261/262

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    Tranquil-C™

    FDA UDI
    NEXUS SPINE, L.L.C.·B6788226390·Cervical Trial, Thin Shaft, 10x16x13, 6 deg

    SYNTHETIC POWDER FREE VINYL PATIENT EXAM GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SYNTHES SYNCAGE EVOLUTION SPACER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OT VERIO PRO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2014

    5MM ARTICNG LNR CUTR/6 ROW BL

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code GDW·November 27, 2007

    TVT-O

    FDA Adverse Event
    Injury ·Product code FTL·October 29, 2012

    Promote Quadra, Sterile EO, Model # / Part #: CD3221-36/100025054, 60019195; CD3223-36P/100013763; CD3239-40/100029115, 100029254, 100037181; CD3239-40Q/100029116, 100029244, 100037115

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018