BEUDAMED
    15 results · 22ms · Sources: EU EUDAMED, US FDA

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    ARTIS ONE

    FDA 510(k)
    FDA Class 2 ·Radiology

    Gibralt

    FDA UDI
    Choice Spine, LP·10885862303110·

    Gibralt®

    FDA UDI
    INNO Holdings, Inc.·M711050021335800·Posterior Cervical, Rod, Prebent, CoCr, 3.5mm x...

    GRANDIO SO FLOW

    FDA 510(k)
    FDA Class 2 ·Dental

    NEXFLEX TOTAL HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    T:SLIM G5 SYSTEM

    FDA Adverse Event
    Injury ·TANDEM DIABETES CARE·Product code OYC·August 13, 2018

    GYNECARE X-TRACT MORCELLATOR

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code HET·May 29, 2013

    OCTRODE LEAD, 60CM LENGTH

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 16, 2011

    5MM, 33CM L-TIP ELECTROSURGICAL PROBE (3BX)

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code GCJ·October 1, 2014

    Enterococcus Screen Agar QUAD Plate

    FDA Enforcement
    Class II ·Terminated·Becton Dickinson & Co.·December 30, 2015

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 20, 2017

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 15, 2017

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 20, 2017

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 11, 2017

    G8

    FDA Adverse Event
    Malfunction ·TOSOH HI-TEC, INC.·Product code PDJ·August 27, 2025