BEUDAMED
    24 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Precision Spine Navigation Instrumentation

    FDA 510(k)
    FDA Class 2 ·Neurology

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694044783·1.6mm X 6mm Profile Zero Autodrive Screw

    Fisherbrand

    FDA UDI
    FISHER SCIENTIFIC COMPANY L.L.C.·00613647020661·FB BLACK NITRILE EXAM GLV, XL

    Origin Short Neck Collared Hip Stem

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215024000·

    VACUTRON

    FDA UDI
    Allied Medical, LLC·00026072010518·

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 11, 2025

    MICROMED PD-8K INSULATION DEFECT DETECTOR

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

    BAHA INTENSO

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·August 17, 2020

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·May 21, 2020

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·August 12, 2020

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·July 8, 2020

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·July 8, 2020

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·June 26, 2020

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·July 8, 2020

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·August 19, 2020

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·July 15, 2020

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·July 24, 2020

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·July 7, 2020

    UV FLASH TRANSFER SETS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·July 27, 2011