BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    STRYKER HERMES-READY TOTAL PERFORMANCE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    Biodesign Anal Fistula Plug, Biodesign Fistula Plug, Biodesign Plastic Surgery Matrix, Biodesign Tissue Graft

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

    SAVI WIRELESS, MODEL PM500

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TT (TRACHEOSTOMY TUBES)

    FDA Adverse Event
    Malfunction ·Product code BTR·October 24, 2017

    FLEXCATH ADVANCE STEERABLE SHEATH

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code DRA·September 17, 2015

    PROGRASP (TM) FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·March 6, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·August 8, 2014