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

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    EKOS PE Endovascular Device with Control System 4.0 (CS4.0)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964074974·Endo Carry-On Procedure Kit

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964077364·The ENDO CARRY-ON Procedure Kit contains all of...

    Apelo® / Apelo® MIS

    FDA UDI
    ATLAS SPINE, INC.·M68120064800000·Collar Sleeve

    SPIRO PRO

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    GRIDLOCK 195 ADHESIVE

    FDA 510(k)
    FDA Class 2 ·Dental

    SYNCHROMED

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·July 27, 2007

    SYNCHROMED

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·July 27, 2007

    SYNCHROMED

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·July 27, 2007

    SYNCHROMED

    FDA Adverse Event
    Death ·MEDTRONIC NEUROMODULATION·Product code LKK·July 27, 2007

    SYNCHROMED

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·July 27, 2007

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·July 16, 2024

    UNK

    FDA Adverse Event
    Injury ·CODMAN AND SHURTLEFF, INC·Product code HCG·June 22, 2017

    UNK

    FDA Adverse Event
    Death ·CODMAN AND SHURTLEFF, INC·Product code HCG·June 22, 2017

    UNK

    FDA Adverse Event
    Malfunction ·CODMAN AND SHURTLEFF, INC·Product code HCG·June 22, 2017

    SYNCHROMED

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·July 27, 2007

    SYNCHROMED

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·July 27, 2007

    SYNCHROMED

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·July 27, 2007

    SYNCHROMED

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·July 27, 2007

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOQ·August 21, 2023