BEUDAMED
    14 results · 24ms · Sources: EU EUDAMED, US FDA

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    FITMATE SERIES

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526189782·***DISC***LEVAMED ACTIVE ANKLE SUP BL

    HALL

    FDA UDI
    Conmed Corporation·10845854002537·LARGE BONE, HALL BLADE, OSCILLATING, 21 X 84.5 ...

    NA

    FDA UDI
    STERILMED, INC.·10888551020800·SAW BLADE OSCILLATING LARGE BONE

    SURGIFLATOR-40

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    DEPUY FEMORAL HEADS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPECTRA WAVEWRITER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 4, 2020

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·April 22, 2013

    MILAGRO

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC·Product code HWC·April 14, 2011

    MINICAP EXTEND LIFE PD TRANSFSET W/TWIST CLAMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·July 3, 2008

    RESTORATION ADM X3 INS

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LZO·May 21, 2019

    BIOLOX HEAD HIP IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code JDI·April 25, 2019

    UNKNOWN BIOLOX HEAD

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·February 13, 2018

    CERASUL, HEAD, M/0, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code JDI·November 4, 2019