BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    FEMORAL ARTERY PRESSURE PAD/DISK

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FLEXISYS

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

    PAEDISCOPE, MODEL # P010A AND PF011A

    FDA 510(k)
    FDA Class 2 ·Neurology

    TRULIANT TIB IMP CR INS STD SZ 3, 11MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·September 5, 2024

    INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·January 14, 2013

    ENDOPATH STEALTH CIR STAPLER

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code KOG·December 3, 2010

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 3, 2014