BEUDAMED
    2,636 results · 21ms · Sources: EU EUDAMED, US FDA

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    PowerHeal 3-layer clear adhesive

    FDA UDI
    ARTHREX, INC.·00810198031539·PowerHeal 3-layer clear adhesive, 4"x4"

    PowerHeal 3-layer clear adhesive

    FDA UDI
    ARTHREX, INC.·00810198031522·PowerHeal 3-layer clear adhesive, 2.3 x 3.5

    PowerHeal 3-layer clear adhesive

    FDA UDI
    ARTHREX, INC.·00810198031546·PowerHeal 3-layer clear adhesive, 6" x 6" "

    PF K-Wire Sleeve, Superior

    FDA UDI
    I.T.S. GmbH·09120116974666·PF K-Wire Sleeve, Superior

    PF K-Wire Sleeve, Inferior

    FDA UDI
    I.T.S. GmbH·09120116974673·PF K-Wire Sleeve, Inferior

    PowerHeal Kit

    FDA UDI
    ARTHREX, INC.·00810198031447·PowerHeal Kit, 4"x4" 3-layer clear adhesive & E...

    PowerHeal Kit

    FDA UDI
    ARTHREX, INC.·00810198031461·PowerHeal Kit, 2.3"x 3.5" 3-layer clear adhesiv...

    PowerHeal Kit

    FDA UDI
    ARTHREX, INC.·00810198031454·PowerHeal Kit, 6"x6" 3-layer & Energel

    PowerHeal Kit

    FDA UDI
    ARTHREX, INC.·00810198031478·PowerHeal Combo Kit, 4"x4", 6"x6", 2.3"x3.5" (3...

    PINNACLE PELVIC FLOOR REPAIR KIT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FTM·January 15, 2009

    HEADFRAME PFK TYPE 1.0 FDA/ROW INTEGRA (FMI)

    FDA UDI
    INSIGHTEC LTD·07290019402442·HEADFRAME PFK TYPE 1.0 FDA/ROW INTEGRA (FMI). M...

    HEADFRAME PFK TYPE 1.1 FDA/ROW INTEGRA (FMI)

    FDA UDI
    INSIGHTEC LTD·07290019402466·HEADFRAME PFK TYPE 1.1 FDA/ROW INTEGRA (FMI). M...

    PFK MODULAR KNEE SYSTEM CURVED TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY-RAYNHAM·Product code JWH·April 18, 2002

    ENDURANT STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·May 6, 2011

    ENDURANT STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·September 28, 2012

    ENDURANT STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code MIH·September 28, 2012

    ENDURANT ILIAC STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·September 28, 2012

    EXABLATE NEURO PATIENT TREATMENT KIT 1.5T GE

    FDA UDI
    INSIGHTEC LTD·07290019402145·EXABLATE NEURO PATIENT TREATMENT KIT 1.5T GE w/...

    EXABLATE NEURO PATIENT TREATMENT KIT 3.0T GE

    FDA UDI
    INSIGHTEC LTD·07290019402169·EXABLATE NEURO PATIENT TREATMENT KIT 3.0T GE w/...

    EXABLATE NEURO PATIENT TREATMENT KIT 3.0T SI

    FDA UDI
    INSIGHTEC LTD·07290019402121·EXABLATE NEURO PATIENT TREATMENT KIT 3.0T SI w/...