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

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    IN VITRO DIAGNOSTIC RADIOIMMUNOASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ARx SAI

    FDA UDI
    Life Spine, Inc.·00190837173791·

    ARx SAI

    FDA UDI
    Life Spine, Inc.·00190837173197·

    ARx SAI

    FDA UDI
    Life Spine, Inc.·00190837189266·

    ARx SAI

    FDA UDI
    Life Spine, Inc.·00190837190736·

    ACTIVECARE DVT ACTIVECARE+SFT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CONTREET-H ANTIMICROBIAL HYDROCOLLOID DRESSING, MODELS 9610 (4 X 4 (10 CM X 10CM), 9613 (6X6 (15CM X 15CM)

    FDA 510(k)
    FDA Unclassified ·Unknown

    ATTAIN ABILITY

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code OJX·October 31, 2012

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR PURITAN BENNETT IRELAND·Product code CBK·March 26, 2014

    SWAN-GANZ BIPOLAR PACING CATHETER FOR SVC INSERTION

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES, PR·Product code LDF·August 24, 2010

    dS Breast 7ch 1.5T

    FDA Enforcement
    Class II ·Ongoing·Philips North America Llc·December 4, 2024