BEUDAMED
    35 results · 25ms · Sources: EU EUDAMED, US FDA

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    MSD BIPOLAR FORCEPS

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

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X0616350·6mm H x 16mm W x 35mm L x 0 degrees XLIF

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111345258·NURSE STETH 30" BLACK

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X061635120·6mm H x 16mm W x 35mm L x 12 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L061635120·6mm H x 16mm W x 35mm L XLIF Trial 12 degree Lo...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X06163580·6mm H x 16mm W x 35mm L x 8 degrees XLIF

    Rapr-Round

    FDA UDI
    STRYKER CORPORATION·07613327261417·

    AXON ECLIPSE CONTROLLER

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC·Product code GWF·October 4, 2013

    KARATS MULTIPURPOSE SOLUTION

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    DEPUY ACROMED VBR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NIM-ECLIPSE® CONTROLLER

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code GWF·February 20, 2018

    AXON ECLIPSE CONTROLLER

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code GWF·December 2, 2013

    NIM-ECLIPSE® PATIENT MODULE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code GWF·December 6, 2017

    PROBE SPK1004 SURGEON CONTROLLED

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code ETN·May 17, 2013

    NIM-ECLIPSE® CONTROLLER

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code GWF·December 14, 2015

    NIM-ECLIPSE® CONTROLLER

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC·Product code GWF·December 9, 2014

    COMPUTER NOTEBOOK (INTERNATIONAL

    FDA Adverse Event
    Malfunction ·MEDTRONIC (CHANGZHOU) MEDICAL DEVICES·Product code GWF·May 9, 2026

    ACCU-CHEK ® AVIVA PLUS TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·April 16, 2013

    VOYAGER NC CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code LOX·April 18, 2011

    AXSYM RUBELLA IGG ANTIBODY

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code LFX·June 17, 2008