BEUDAMED
    10 results · 27ms · Sources: EU EUDAMED, US FDA

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    EMIT-TOX SERUM BENZODIAZEPINE ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517663993·CoRoent® Small Interlock, 16x19x16mm 7°

    N.A.

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011790736010·dinamique m Bracket, 0°Torque, +3°Angulation, t...

    Disposable Powder Free Nitrile Examination Glove,Blue Color, Tested For Use With Chemotherapy Drugs

    FDA 510(k)
    FDA Class 1 ·General Hospital

    POWER INFUSER, MODEL M100B-3A

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HRS·May 5, 2014

    EXTERNAL PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA INC.·Product code DTE·October 15, 2012

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·August 10, 2010

    MENTOR SMOOTH ROUND MODERATE PLUS PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·May 20, 2019

    MENTOR SMOOTH ROUND MODERATE PLUS PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·May 20, 2019