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

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    Truliant Porous Femoral Components

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TRULIANT

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·July 14, 2025

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·October 6, 2021

    Bernafon

    FDA UDI
    Bernafon AG·05711584075999·OASIS NXT 2017.1 CUSTOM

    ASC TRIPORT LAPAROSCOPIC ACCESS DEVICE MODEL TPRT-02-01 (WA58000T), ASC QUADPORT LAPAROSCOPIC ASSCESS DEVICE QPRT-01 (WA

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    MODEL 7340 ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·October 17, 2014

    PAINSMART IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·June 6, 2013

    ECHELON*FLEX60 COMPACT ARTICULATING ENDOSCOPIC LINEAR CUTTER, 60 MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 27, 2011