BEUDAMED
    15 results · 23ms · Sources: EU EUDAMED, US FDA

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    Fully Automatic Electronic Blood Pressure Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741622300·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674162230060·

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X1622300·16mm H x 22mm W x 30mm L x 0 degrees XLIF

    Epimed

    FDA UDI
    EPIMED INTERNATIONAL, INC·00818788020444·22g RW x 3.0" Blunt Nerve Block Needle

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X162230120·16mm H x 22mm W x 30mm L x 12 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L162230120·16mm H x 22mm W x 30mm L XLIF Trial 12 degree L...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X16223080·16mm H x 22mm W x 30mm L x 8 degrees XLIF

    MR FIBER OPTIC INTUBATING LARYNGOSCOPE HANDLE, SHORT, MODEL 310002

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    NUGARD NITILE GREY COLOR

    FDA 510(k)
    FDA Class 1 ·General Hospital

    OT VERIO2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 9, 2018

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 11, 2013

    TOTAL ASR ACET IMP SIZE 56

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD.·Product code KWA·July 7, 2011

    HI-TORQUE STEELCORE 18 GUIDE WIRE WITH MICROGLIDE COATING

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code DQX·September 16, 2008

    BIOMET StageOne, Hip Cement Spacer Mold w/Reinforcement, 9 X 125 MM, 51 MM, Silicone, Sterile, Item 431209.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·April 15, 2020