BEUDAMED
    13 results · 22ms · Sources: EU EUDAMED, US FDA

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    MICRUSFRAME 10/18, DELTAFILL 18, DELTAXSFT 10, GALAXY G3 FILL/XSFT STRETCH RESISTANT MICROCOIL DELIVERY SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Neurology

    Leg Bag

    FDA UDI
    C. R. Bard, Inc.·00801741050794·Dispoz-A-Bag, Leg Bag with Flip-Flo Drainage Va...

    HHM

    FDA UDI
    Oticon A/S·05707131286710·H100V2, MINIRITE 312 WL CBE HHM

    MAYFIELD MR/CT SKULL CLAMP, MODEL 4-0-A-1104

    FDA 510(k)
    FDA Class 2 ·Neurology

    MERIT MANIFOLD WITH INTEGRATED TRANSDUCER, MODEL 203LTCHN-R; 503LTCHN-R; 203LTPHN-R,203LTCHWN-R; 503LTCHWN-R; 203L

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MAGEC® SPINAL BRACING AND DISTRACTION SYSTEM

    FDA Adverse Event
    Injury ·NUVASIVE SPECIALIZED ORTHOPEDICS, INC.·Product code PGN·August 16, 2016

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·August 26, 2016

    INTELLIVUE MULTI-MEASUREMENT MODULE X3

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code MHX·June 12, 2025

    PRECICE® INTRAMEDULLARY LIMB LENGTHENING ROD

    FDA Adverse Event
    Injury ·NUVASIVE SPECIALIZED ORTHOPEDICS, INC.·Product code HSB·June 28, 2016

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·November 10, 2016

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·October 7, 2014

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC·Product code DRM·May 30, 2013

    SGL TRIG WIRE COLLET 0.7-1.8MM

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·June 7, 2011