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

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    EARBEAR OTOSCOPE

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    PERRY XTENDA CUFF SURGICAL GLOVES

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    VISI-STREP

    FDA 510(k)
    FDA Class 1 ·Microbiology

    MODULUS-STRUM. - ESTRATTORE

    FDA Adverse Event
    Malfunction ·LIMACORPORATE S.P.A.·Product code KWY·August 26, 2021

    UNKNOWN HIP STEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JDI·January 10, 2013

    ITREL 3

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code LGW·November 5, 2010

    LIGAMAX CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·July 7, 2014

    FEMORAL MODULAR HEAD - M Ø32MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code LZO·August 26, 2021

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021