BEUDAMED
    14 results · 20ms · Sources: EU EUDAMED, US FDA

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    SMITH & NEPHEW COMPRESSION HIP SCREW SYSTEM, INTRAMEDULLARY HIP SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993289·anteriors; shade B4; mould UBS

    FastStroke, CT Perfusion 4D

    FDA 510(k)
    FDA Class 2 ·Radiology

    PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code IOR·March 7, 2013

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·February 7, 2011

    PROTECTA XT DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·August 8, 2014

    DURAL ALPHA INSERT W RIM II/32

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code LPH·March 12, 2019

    DURASUL, ALPHA INSERT, HOODED, II/32

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LPH·September 28, 2018

    METASUL, ALPHA INSERT, JJ/28

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·February 4, 2019

    DURASUL, ALPHA INSERT, KK/36

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code JDI·March 13, 2018

    COCR HEAD 32/ 0 'M' 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code JDI·June 4, 2019

    DURASUL, ALPHA INSERT, LL/36

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code JDI·April 29, 2019

    DURASUL, ALPHA INSERT, HOODED, KK/32

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code LPH·June 15, 2018