BEUDAMED
    16 results · 29ms · Sources: EU EUDAMED, US FDA

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    SARNS 9000 PERFUSION SYSTEM W/ALERT ONLY LEVEL

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526785045·EPICOMED ELB SUPPORT SAND V

    Mariner

    FDA UDI
    Seaspine Orthopedics Corporation·10889981134501·Non-Ratcheting Pineapple Handle, Cannulated, A/O

    3M™ Unitek™

    FDA UDI
    3M UNITEK CORPORATION·00652221111234·3M™ Unitek™ Prestige Universal Cutter, Long Han...

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M930790081500·Scoville Retractor w/Suction 5mm 8FR (SS Thumb)

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M93079008100C0·8mm Scoville Retractor w/ 10FR Suction

    PERCUTANEOUS DISCECTOMY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AS/3 ANESTHESIA MONTIOR WITH S-ANE99(A)/L-ARK99(A)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·June 27, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·November 16, 2010

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 12, 2012

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 1, 2024

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 1, 2024

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 1, 2024

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 1, 2024

    HEARTMATE 3 LVAS IMPLANT KIT

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·August 24, 2022