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

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    JOWIRE ASAHI PTCA CATHETER GUIDE WIRES, MODELS AG145300,141300,142300,132200,14M350,14M345,14M360,143390,141002

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    T1 LINE

    FDA UDI
    SIRONA Dental Systems GmbH·E27660312770·T1 LINE H 40 L

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496031277·MISS RELAX 100 SHEER, SIZE M, GLACE, GRADUATED ...

    HARD RELINER

    FDA 510(k)
    FDA Class 2 ·Dental

    TRIFLANGE ACETABULAR CUP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KWQ·November 11, 2015

    APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KWQ·November 11, 2015

    APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KWQ·November 11, 2015

    APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KWQ·November 11, 2015

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·February 5, 2025

    IPC® STYLUS TRANSNASAL BUR

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code ERL·February 6, 2015

    IPC® HANDPIECE - XPS® STRAIGHTSHOT® M4

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC·Product code ERL·June 19, 2015

    XPS® BUR

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code EQJ·September 8, 2017

    ACCY EF201 IPC FOOT CONTROL ROHS

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code HBE·September 9, 2014

    XPS® BUR - UNKNOWN

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code EQJ·June 17, 2016

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 16, 2011

    CONMED

    FDA Adverse Event
    CONMED·Product code GEI·April 4, 2006

    SETROX S 53

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO.·Product code DTB·April 18, 2008

    XOM UNKNOWN ENDO

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED, INC.·Product code EQJ·May 8, 2015

    XPS® HANDPIECE - UNKNOWN

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code HBE·November 8, 2016