BEUDAMED
    43 results · 39ms · Sources: EU EUDAMED, US FDA

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    PICCOLO COMPOSITE NAILING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Surgical Instrument

    FDA UDI
    Jeil Medical Corporation·08809282815553·

    MicroSelectron Digital

    FDA UDI
    Nucletron B.V.·08717213015395·microSelectron Transfer Tube for 5F Flexibles (5)

    Summa Orthopaedics System Surgical Instrument

    FDA UDI
    Jeil Medical Corporation·08806390864084·

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523166312·Initia T3 Acetabular Hemispherical Shell, No Ho...

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523103690·Hemispherical Shell, No Hole, 56mm

    ARROW-TREROTOLA PERCUTANEOUS THROMBOLYTIC DEVICE OR PTD

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VARIAX ELBOW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Trabecular Metal®

    FDA UDI
    Zimmer, Inc.·00889024130012·

    Trabecular Metal®

    FDA UDI
    Zimmer, Inc.·00889024130005·

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·July 8, 2014

    CUSTOM PROXIMAL FEMUR IMPLANT

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code KRO·December 23, 2014

    CUSTOMER PROXIMAL FEMUR REPLACEMENT IMPLANT

    FDA Adverse Event
    Injury ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code KRO·December 19, 2014

    CUSTOM PROXIMAL FEMUR REPLACEMENT IMPLANT

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code JWH·January 8, 2015

    SCREW, 2.0X16MM X-DRV LOCKING

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·May 14, 2013

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·September 23, 2014

    4.0MM AGGRESSIVE PLUS CUTTER, FORMULA (5BX)

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY PUERTO RICO·Product code HRX·May 18, 2011

    CUSTOM DISTAL FEMORAL IMPLANT

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code KRO·December 23, 2014

    UNK- NON- STANMORE HIP REPLACEMENT IMPLANT

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code KRO·June 25, 2015

    CUSTOM PROXIMAL FEMUR REPLACEMENT IMPLANT

    FDA Adverse Event
    Malfunction ·STANMORE IMPLANTS WORLDWIDE LTD.·Product code KRO·December 19, 2014