BEUDAMED
    389 results · 34ms · Sources: EU EUDAMED, US FDA

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    ARTERIAL CATHETER

    FDA Adverse Event
    Injury ·DLP, INC.·Product code DWF·July 8, 1996

    ARTERIAL CATHETER

    FDA Adverse Event
    Injury ·DLP, INC.·Product code DWF·July 8, 1996

    FEMORAL VENOUS DRAINAGE CANNULA

    FDA Adverse Event
    Injury ·DLP, INC.·Product code DWF·February 27, 1997

    FEMORAL VENOUS DRAINAGE CANNULA

    FDA Adverse Event
    Injury ·DLP, INC.·Product code DWF·February 27, 1997

    DLP

    FDA Adverse Event
    Injury ·DLP, INC.·Product code DYG·September 1, 1999

    PRESSURE DISPLAY SET

    FDA Adverse Event
    Injury ·DLP, INC·Product code DRS·February 14, 1996

    DLP 10003 ADAPTER Y TYPE

    FDA Adverse Event
    Injury ·DLP INC./INRAD·Product code DTL·February 12, 1997

    MEDTRONIC/DLP

    FDA Adverse Event
    DLP. DIVISION MEDTRONIC, INC.·Product code DWF·July 6, 1998

    MEDTRONIC

    FDA Adverse Event
    Malfunction ·DLP, DIV MEDTRONIC, INC.·Product code DWF·September 18, 1998

    MEDTRONIC/DLP

    FDA Adverse Event
    Malfunction ·DLP, DIV. MEDTRONIC, INC.·Product code DWF·July 2, 1998

    PROSTAR XL SUTURE-MEDIATED CLOSURE

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·April 15, 2011

    DSI

    FDA UDI
    SLP INC·07290013820273·

    Sleepsense

    FDA UDI
    SLP INC·07290013385017·

    Sleepsense

    FDA UDI
    SLP INC·07290012144325·

    Natus

    FDA UDI
    SLP INC·07290013818843·

    Grass

    FDA UDI
    SLP INC·07290013819789·

    Sleepsense

    FDA UDI
    SLP INC·07290013385024·

    DSI

    FDA UDI
    SLP INC·07290013820266·

    Sleepsense

    FDA UDI
    SLP INC·07290013818911·

    Grass

    FDA UDI
    SLP INC·07290013819802·