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

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    KODAK MN-R 2000 CASSETTE

    FDA 510(k)
    FDA Class 2 ·Radiology

    P.F.C. SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295238713·P.F.C. SIGMA STABILIZED TIBIAL INSERT TRIAL SZ ...

    HI-TORQUE WHISPER VIEW GUIDE WIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    WELL LIFE Wireless TENS/EMS Stimulator, Models WR-2605/2605A

    FDA 510(k)
    FDA Class 2 ·Neurology

    STRYKER GO BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·January 17, 2013

    UNKNOWN INTERNAL STIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·July 28, 2014

    CODEMASTER XL+

    FDA Adverse Event
    Malfunction ·AGILENT TECHNOLOGIES, INC.·Product code LDD·January 10, 2011