BEUDAMED
    15 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    ArgenIS Titanium Abutments

    FDA 510(k)
    FDA Class 2 ·Dental

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741724300·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674172430060·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694027250·2.4mm X 30mm Cannulated Headless Screw

    G8 Curved Cup Inserter - TBall

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215057800·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694068987·Cannulated 2.4 x 30mm Headless Screw Sterile Qty 5

    ZOLL PEDIPADZ REDUCED ENERGY ELECTRODE

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    TYCO ELECTRONICS ELECTROCARDIOGRAPH (ECG) LEADWIRE SET

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·August 8, 2016

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 3, 2025

    LIFEPAK(R) 1000 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·July 10, 2015

    LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·December 23, 2014

    VASOVIEW HEMOPRO 2

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·October 9, 2014

    AUTOTOME? RX 44

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code KNS·June 17, 2013

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code LZG·June 17, 2011