BEUDAMED
    11 results · 25ms · Sources: EU EUDAMED, US FDA

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    3M MODULAR SHOULDER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    METAFIX FEMORAL STEM FOR HEMI-ARTHROPLASTY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    P.O.G.S. 3.3 PORTABLE OXYGEN GENERATOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DRILL BIT Ø2.5 L110/85 2FLUTE

    FDA Adverse Event
    Malfunction ·SYNTHES BETTLACH·Product code HWE·February 8, 2017

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNS·June 7, 2006

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNS·June 7, 2006

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KNS·June 7, 2006

    ULTRACISION SURG DEV, BLADES 10MM REUSABLE, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GEO·June 19, 2006

    CE INTERMATE LV 50, 24 PACK, 50126

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·December 10, 2010

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS INC·Product code LYJ·January 17, 2013

    PRECISION SPECTRA®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 8, 2014