BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    Valeo C Spacer System, Valeo II C IBF Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526550131·GENUMEDI PT KNEE SUP SILVER L EW IV

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814213·GENUMEDI PT SILVER L IV

    PRIMADO2 TOTAL SURGICAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    GUIDEWIRES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GYNECARE MORCELLEX* TISSUE MORCELLATOR

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code HET·June 3, 2013

    ENDOPATH** XCEL* TROCAR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·June 28, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 3, 2008

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code HBC·March 26, 2018