BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756591584·MINOR LAP PACK

    DENTAL ORAL CARE SYSTEMS & COMPONENTS

    FDA 510(k)
    FDA Class 2 ·Dental

    INJECTION CAP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LEAD EXTRACTION BYRD POLYPROPYLENE EXTRA LONG DILATOR SHEATH SET

    FDA Adverse Event
    Injury ·COOK VANDERGRIFT INC·Product code GCC·January 22, 2021

    UNIVERSAL MODULAR ELECTRIC/BATTERY DOUBLE

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL S.A.·Product code HAB·April 25, 2014

    LOVENOX

    FDA Adverse Event
    Malfunction ·SANOFI AVENTIS·Product code FMF·October 26, 2010

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code CBK·December 27, 2012

    LEAD EXTRACTION BYRD POLYPROPYLENE DILATOR SHEATH SET

    FDA Adverse Event
    Malfunction ·COOK VANDERGRIFT INC·Product code GCC·March 9, 2022