BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    XiniWave II Model ECS322P

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    UHEAD

    FDA UDI
    Stryker GmbH·00886385013602·Instrument Tray Assembly

    ASNIS MICRO CANNULATED SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARCTIC SUN TEMPERATURE MANAGEMENT SYSTEM, MODEL 5000

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·April 27, 2018

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code NIQ·April 27, 2018

    CLICKX LOCKCAP F/498.571V TAV

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·June 14, 2013

    NI

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·July 8, 2011

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM 9.75CM

    FDA Adverse Event
    Injury ·BIOENTERICS CORP·Product code LTI·September 18, 2008

    CHROMID® CARBA SMART

    FDA Adverse Event
    Malfunction ·BIOMERIEUX S.A.·Product code JSO·August 23, 2018