BEUDAMED
    9 results · 30ms · Sources: EU EUDAMED, US FDA

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    INVISION TOTAL ANKLE REVISION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526550162·GENUMEDI PT KNEE SUP SILVER L EW VII

    TISSU TRANS FILTRON SYRINGE FILL

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    PROXIS SYSTEM, MODEL EPS 101

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SCREWDRIVER SHAFT, COMPRESSION T2 TIBIA 3.5 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HXX·July 27, 2012

    ESOPHYX Z

    FDA Adverse Event
    Injury ·ENDOGASTRIC SOLUTIONS, INC.·Product code ODE·June 22, 2017

    SUMMIT DUOFIX TAP SZ5 STD OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·October 4, 2014

    BHR

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPAEDICS LTD·Product code NXT·June 3, 2013

    EASYPUMP

    FDA Adverse Event
    Malfunction ·I-FLOW CORP.·Product code MEB·May 26, 2011