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

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    NICO TRIOwand

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

    VITEK 2 STRPTOCOCCUS AMPICILLIN

    FDA 510(k)
    FDA Class 2 ·Microbiology

    DISPOSABLE GAS SAMPLING LINE WITH AND WITHOUT IN-LINE FILTER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    WEREWOLF RF 20000 CONTROLLER

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORP.·Product code GEI·June 29, 2020

    UNKNOWN_FRO_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER LEIBINGER FREIBURG·Product code JEY·October 10, 2014

    UNKNOWN

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code FTL·May 31, 2013

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·July 12, 2011

    MAGNETOM Verio Dot Upgrade. Model Number: 10684334.

    FDA Enforcement
    Class I ·Ongoing·Siemens Medical Solutions USA, Inc·October 8, 2025