BEUDAMED
    25 results · 28ms · Sources: EU EUDAMED, US FDA

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    Portable X-ray System (Model: MiniX-V, Mini X-S)

    FDA 510(k)
    FDA Class 2 ·Dental

    SYNTHES BRAINLAB TRAUMA COMPATIBLE INSTRUMENTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FUKUDA DENSHI DYNASCOPE MODEL DS-7000/7000M PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·June 21, 2013

    SELECTA II

    FDA Adverse Event
    Injury ·LUMENIS, INC.·Product code GEX·July 28, 2011

    GE OEC 9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 19, 2008

    S-ROM*SLEEVE PRX ZT HA 18F-XXL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 181891·Product code MEH·January 31, 2012

    S/C TRIAL HANDLE ANGLED

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 181891·Product code HWA·October 12, 2018

    SUMMIT DUOFIX TAP SZ8 STD OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 181891·Product code LPH·May 3, 2019

    TRI-LOCK BPS SZ 8 HI OFFSET

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 181891·Product code KWA·April 22, 2019

    DEPUY CMW 2 20G

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 181891·Product code LOD·June 18, 2019

    UNKNOWN KNEE IMPLANT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 181891·Product code JWH·April 3, 2019

    UNKNOWN HIP ACETABULAR LINERS

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 181891·Product code KWA·May 17, 2019

    PINNACLE 300 ACET CUP 58MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 181891·Product code LPH·May 16, 2019

    TRI-LOCK BPS SZ 2 HI OFFSET

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 181891·Product code KWA·January 7, 2019

    UNKNOWN HIP ACETABULAR LINERS

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 181891·Product code KWA·January 8, 2019

    UNKNOWN HIP FEMORAL STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 181891·Product code JDI·April 3, 2018

    AML HIGH OFFSET LG STAT 16.5MM

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC. 181891·Product code JDI·January 12, 2018

    SIGMA PS CEM FEM SZ4N R

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 181891·Product code JWH·September 25, 2019

    UNKNOWN SHOULDER NON-LOCKING SCREW

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 181891·Product code HWC·September 13, 2019