BEUDAMED
    9 results · 23ms · Sources: EU EUDAMED, US FDA

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    V8 Diagnostic Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    PRS Plate

    FDA UDI
    I.T.S. GmbH·09120034302824·PRS Plate, 5-Hole, Curved, R88

    IMPAX NEXT GENERATION

    FDA 510(k)
    FDA Class 2 ·Radiology

    RIGID GAS PERMEABLE CONTACT LENS SOLUTION

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    BELT CLIP PUMP CLEAR

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·October 29, 2014

    ENDOPATH** XCEL* TROCAR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·August 15, 2011

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·July 8, 2013

    Sheep Blood, Defibrinated - Catalog Number 211945, Unit 15 ml.

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code JSO·July 2, 2004

    UNK SHOULDER HUMERAL STEM DELTA XTEND

    FDA Adverse Event
    Malfunction ·DEPUY IRELAND·Product code HSD·June 18, 2025