BEUDAMED
    19 results · 24ms · Sources: EU EUDAMED, US FDA

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    Upper Arm Blood Pressure Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    URITEK TC-101 URINE ANALYZER, URINE REAGENT STRIPS 10, MODELS TC-101, URS-10

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    GE LIGHTSPEED ACT FP16

    FDA 510(k)
    FDA Class 2 ·Radiology

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, CERVICAL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code ODP·September 29, 2015

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, CERVICAL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code ODP·September 29, 2015

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, CERVICAL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code ODP·September 29, 2015

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, CERVICAL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code ODP·September 29, 2015

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, CERVICAL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code ODP·September 29, 2015

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, CERVICAL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code ODP·September 29, 2015

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, CERVICAL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code ODP·September 29, 2015

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, CERVICAL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code ODP·September 29, 2015

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, CERVICAL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code ODP·September 29, 2015

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, CERVICAL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code ODP·September 29, 2015

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, CERVICAL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code ODP·September 29, 2015

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, CERVICAL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code ODP·September 29, 2015

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·June 26, 2013

    STENOSCOP

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 27, 2011

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code ILS·October 22, 2014

    TrueBeam Radiotherapy Delivery System version 2.0 and 2.5 EDGE Radiotherapy Delivery System version 2.0 and 2.5 Product Usage: The TrueBeam delivery systems are intended to provide radiotherapy and stereotactic radiosurgery for lesions, tumors, and conditions anywhere in the body where radiation treatment is indicated.

    FDA Enforcement
    Class II ·Terminated·Varian Medical Systems·October 10, 2018