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

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    Cervical Spine Truss System (CSTS) Interbody Fusion Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Wet-Field® Eraser

    FDA UDI
    Beaver-Visitec International, Inc.·30886158010532·20-23 GA Tapered Blunt Tip

    UNITRAY ABC SSP

    FDA Adverse Event
    Malfunction ·Product code MZI·September 26, 2013

    ENDO WINDOW HIGH FREQUENCY ELECTROCAUTERY DEVICE, MODEL EW018

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    CARDIOSCOPE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ABC SSP UNITRAY KIT WITH TAQ POLYMERASE

    FDA Adverse Event
    Malfunction ·LIFE TECHNOLOGIES CORPORATION·Product code MZI·December 26, 2013

    ABC SSP UNITRAY KIT WITH TAQ POLYMERASE

    FDA Adverse Event
    Malfunction ·LIFE TECHNOLOGIES CORPORATION·Product code MZI·December 26, 2013

    ABC SSP UNITRAY KIT WITH TAQ POLYMERASE

    FDA Adverse Event
    Malfunction ·LIFE TECHNOLOGIES CORPORATION·Product code MZI·December 26, 2013

    ABC SSP UNITRAY KIT WITH TAQ POLYMERASE

    FDA Adverse Event
    Malfunction ·LIFE TECHNOLOGIES CORPORATION·Product code MZI·December 26, 2013

    ABC SSP UNITRAY KIT WITH TAQ POLYMERASE

    FDA Adverse Event
    Malfunction ·LIFE TECHNOLOGIES CORPORATION·Product code MZI·December 26, 2013

    ABC SSP UNITRAY KIT WITH TAQ POLYMERASE

    FDA Adverse Event
    Malfunction ·LIFE TECHNOLOGIES CORPORATION·Product code MZI·December 26, 2013

    ABC SSP UNITRAY KIT WITH TAQ POLYMERASE

    FDA Adverse Event
    Malfunction ·LIFE TECHNOLOGIES CORPORATION·Product code MZI·December 26, 2013

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 31, 2024

    MESH-COMPOSIX

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·August 17, 2011

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    JUMAO HEALTHCARE EQUIPMENT·Product code IOR·November 3, 2014

    ARTICULEZE M HEAD 36MM -2

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·July 11, 2013

    CD HORIZON® SOLERA® VOYAGER¿ SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HWE·May 20, 2025

    CD HORIZON® SOLERA® VOYAGER¿ SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HWE·May 20, 2025

    CD HORIZON® SOLERA® VOYAGER¿ SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HWE·May 20, 2025

    CD HORIZON® SOLERA® VOYAGER¿ SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HWE·May 20, 2025